Canonical Allele Identifier: CA2680892389

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157190016-T-TATCATTAAGCTGTA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190016_157190017insATCATTAAGCTGTA , CM000668.2:g.157190016_157190017insATCATTAAGCTGTA	GRCh38
NC_000006.11:g.157511150_157511151insATCATTAAGCTGTA , CM000668.1:g.157511150_157511151insATCATTAAGCTGTA	GRCh37
NC_000006.10:g.157552842_157552843insATCATTAAGCTGTA	NCBI36
NG_032093.1:g.417087_417088insATCATTAAGCTGTA
NG_032093.2:g.417087_417088insATCATTAAGCTGTA
NG_066624.1:g.418991_418992insATCATTAAGCTGTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3900-22_3900-21insATCATTAAGCTGTA	ENSP00000055163.8:n.3900-22_3900-21insATCATTAAGCTGTA
ENST00000414678.8:c.3969-22_3969-21insATCATTAAGCTGTA	ENSP00000412835.3:n.3969-22_3969-21insATCATTAAGCTGTA
ENST00000637015.2:c.4188-22_4188-21insATCATTAAGCTGTA	ENSP00000489729.2:n.4188-22_4188-21insATCATTAAGCTGTA
ENST00000346085.10:c.3939-22_3939-21insATCATTAAGCTGTA	ENSP00000344546.5:n.3939-22_3939-21insATCATTAAGCTGTA
ENST00000350026.10:c.3651-22_3651-21insATCATTAAGCTGTA	ENSP00000055163.7:n.3651-22_3651-21insATCATTAAGCTGTA
ENST00000414678.7:c.2217-22_2217-21insATCATTAAGCTGTA	ENSP00000412835.2:n.2217-22_2217-21insATCATTAAGCTGTA
ENST00000635849.1:c.1380-22_1380-21insATCATTAAGCTGTA	ENSP00000490948.1:n.1380-22_1380-21insATCATTAAGCTGTA
ENST00000635957.1:c.1014-25_1014-24insATCATTAAGCTGTA	ENSP00000490385.1:n.1014-25_1014-24insATCATTAAGCTGTA
ENST00000636930.2:c.4059-22_4059-21insATCATTAAGCTGTA MANE Select	ENSP00000490491.2:n.4059-22_4059-21insATCATTAAGCTGTA
ENST00000636940.1:n.2056-22_2056-21insATCATTAAGCTGTA
ENST00000637015.1:c.1427-22_1427-21insATCATTAAGCTGTA
ENST00000637568.1:c.1341-22_1341-21insATCATTAAGCTGTA
ENST00000637741.1:n.725-22_725-21insATCATTAAGCTGTA
ENST00000637810.1:c.1401-22_1401-21insATCATTAAGCTGTA	ENSP00000489636.1:n.1401-22_1401-21insATCATTAAGCTGTA
ENST00000637904.1:c.1560-22_1560-21insATCATTAAGCTGTA	ENSP00000490550.1:n.1560-22_1560-21insATCATTAAGCTGTA
ENST00000647938.1:c.3690-22_3690-21insATCATTAAGCTGTA	ENSP00000498155.1:n.3690-22_3690-21insATCATTAAGCTGTA
ENST00000346085.9:c.3690-22_3690-21insATCATTAAGCTGTA	ENSP00000344546.4:n.3690-22_3690-21insATCATTAAGCTGTA
ENST00000350026.9:c.3651-22_3651-21insATCATTAAGCTGTA	ENSP00000055163.7:n.3651-22_3651-21insATCATTAAGCTGTA
ENST00000414678.6:c.2217-22_2217-21insATCATTAAGCTGTA	ENSP00000412835.2:n.2217-22_2217-21insATCATTAAGCTGTA
NM_017519.2:c.3651-22_3651-21insATCATTAAGCTGTA	NP_059989.2:n.3651-22_3651-21insATCATTAAGCTGTA
NM_020732.3:c.3690-22_3690-21insATCATTAAGCTGTA	NP_065783.3:n.3690-22_3690-21insATCATTAAGCTGTA
XM_005267069.3:c.3810-22_3810-21insATCATTAAGCTGTA	XP_005267126.2:n.3810-22_3810-21insATCATTAAGCTGTA
XM_011535984.1:c.2889-22_2889-21insATCATTAAGCTGTA	XP_011534286.1:n.2889-22_2889-21insATCATTAAGCTGTA
XM_011535985.1:c.2709-22_2709-21insATCATTAAGCTGTA	XP_011534287.1:n.2709-22_2709-21insATCATTAAGCTGTA
XM_011535986.1:c.2469-22_2469-21insATCATTAAGCTGTA	XP_011534288.1:n.2469-22_2469-21insATCATTAAGCTGTA
XM_011535987.1:c.2088-22_2088-21insATCATTAAGCTGTA	XP_011534289.1:n.2088-22_2088-21insATCATTAAGCTGTA
XM_011535988.1:c.951-22_951-21insATCATTAAGCTGTA	XP_011534290.1:n.951-22_951-21insATCATTAAGCTGTA
NM_001346813.1:c.3810-22_3810-21insATCATTAAGCTGTA	NP_001333742.1:n.3810-22_3810-21insATCATTAAGCTGTA
NM_001363725.1:c.1560-22_1560-21insATCATTAAGCTGTA	NP_001350654.1:n.1560-22_1560-21insATCATTAAGCTGTA
XM_011535984.2:c.4020-22_4020-21insATCATTAAGCTGTA	XP_011534286.2:n.4020-22_4020-21insATCATTAAGCTGTA
XM_011535988.3:c.951-22_951-21insATCATTAAGCTGTA	XP_011534290.1:n.951-22_951-21insATCATTAAGCTGTA
XM_017011103.2:c.3921-22_3921-21insATCATTAAGCTGTA	XP_016866592.1:n.3921-22_3921-21insATCATTAAGCTGTA
XM_017011104.1:c.3891-22_3891-21insATCATTAAGCTGTA	XP_016866593.1:n.3891-22_3891-21insATCATTAAGCTGTA
XM_017011105.2:c.3861-22_3861-21insATCATTAAGCTGTA	XP_016866594.1:n.3861-22_3861-21insATCATTAAGCTGTA
XM_017011106.2:c.3732-22_3732-21insATCATTAAGCTGTA	XP_016866595.1:n.3732-22_3732-21insATCATTAAGCTGTA
XM_017011107.2:c.3711-22_3711-21insATCATTAAGCTGTA	XP_016866596.1:n.3711-22_3711-21insATCATTAAGCTGTA
XR_002956289.1:n.4103-22_4103-21insATCATTAAGCTGTA
NM_001363725.2:c.1560-22_1560-21insATCATTAAGCTGTA	NP_001350654.1:n.1560-22_1560-21insATCATTAAGCTGTA
NM_001371656.1:c.3939-22_3939-21insATCATTAAGCTGTA	NP_001358585.1:n.3939-22_3939-21insATCATTAAGCTGTA
NM_001374820.1:c.3939-22_3939-21insATCATTAAGCTGTA	NP_001361749.1:n.3939-22_3939-21insATCATTAAGCTGTA
NM_001374828.1:c.4059-22_4059-21insATCATTAAGCTGTA MANE Select	NP_001361757.1:n.4059-22_4059-21insATCATTAAGCTGTA
NM_017519.3:c.3900-22_3900-21insATCATTAAGCTGTA	NP_059989.3:n.3900-22_3900-21insATCATTAAGCTGTA