Canonical Allele Identifier: CA571903957

Gene: ARID1B

Linked Data

• dbSNP Id: rs1460478903
• gnomAD v2: 6-157511141-CATT-C
• gnomAD v4: 6-157190007-CATT-C
• MyVariant Identifiers: chr6:g.157511142_157511144del (hg19) ; chr6:g.157190008_157190010del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190009_157190011del , CM000668.2:g.157190009_157190011del	GRCh38
NC_000006.11:g.157511143_157511145del , CM000668.1:g.157511143_157511145del	GRCh37
NC_000006.10:g.157552835_157552837del	NCBI36
NG_032093.1:g.417080_417082del
NG_032093.2:g.417080_417082del
NG_066624.1:g.418984_418986del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3900-29_3900-27del	ENSP00000055163.8:n.3900-29_3900-27del
ENST00000414678.8:c.3969-29_3969-27del	ENSP00000412835.3:n.3969-29_3969-27del
ENST00000637015.2:c.4188-29_4188-27del	ENSP00000489729.2:n.4188-29_4188-27del
ENST00000346085.10:c.3939-29_3939-27del	ENSP00000344546.5:n.3939-29_3939-27del
ENST00000350026.10:c.3651-29_3651-27del	ENSP00000055163.7:n.3651-29_3651-27del
ENST00000414678.7:c.2217-29_2217-27del	ENSP00000412835.2:n.2217-29_2217-27del
ENST00000635849.1:c.1380-29_1380-27del	ENSP00000490948.1:n.1380-29_1380-27del
ENST00000635957.1:c.1014-32_1014-30del	ENSP00000490385.1:n.1014-32_1014-30del
ENST00000636930.2:c.4059-29_4059-27del MANE Select	ENSP00000490491.2:n.4059-29_4059-27del
ENST00000636940.1:n.2056-29_2056-27del
ENST00000637015.1:c.1427-29_1427-27del
ENST00000637568.1:c.1341-29_1341-27del
ENST00000637741.1:n.725-29_725-27del
ENST00000637810.1:c.1401-29_1401-27del	ENSP00000489636.1:n.1401-29_1401-27del
ENST00000637904.1:c.1560-29_1560-27del	ENSP00000490550.1:n.1560-29_1560-27del
ENST00000647938.1:c.3690-29_3690-27del	ENSP00000498155.1:n.3690-29_3690-27del
ENST00000346085.9:c.3690-29_3690-27del	ENSP00000344546.4:n.3690-29_3690-27del
ENST00000350026.9:c.3651-29_3651-27del	ENSP00000055163.7:n.3651-29_3651-27del
ENST00000414678.6:c.2217-29_2217-27del	ENSP00000412835.2:n.2217-29_2217-27del
NM_017519.2:c.3651-29_3651-27del	NP_059989.2:n.3651-29_3651-27del
NM_020732.3:c.3690-29_3690-27del	NP_065783.3:n.3690-29_3690-27del
XM_005267069.3:c.3810-29_3810-27del	XP_005267126.2:n.3810-29_3810-27del
XM_011535984.1:c.2889-29_2889-27del	XP_011534286.1:n.2889-29_2889-27del
XM_011535985.1:c.2709-29_2709-27del	XP_011534287.1:n.2709-29_2709-27del
XM_011535986.1:c.2469-29_2469-27del	XP_011534288.1:n.2469-29_2469-27del
XM_011535987.1:c.2088-29_2088-27del	XP_011534289.1:n.2088-29_2088-27del
XM_011535988.1:c.951-29_951-27del	XP_011534290.1:n.951-29_951-27del
NM_001346813.1:c.3810-29_3810-27del	NP_001333742.1:n.3810-29_3810-27del
NM_001363725.1:c.1560-29_1560-27del	NP_001350654.1:n.1560-29_1560-27del
XM_011535984.2:c.4020-29_4020-27del	XP_011534286.2:n.4020-29_4020-27del
XM_011535988.3:c.951-29_951-27del	XP_011534290.1:n.951-29_951-27del
XM_017011103.2:c.3921-29_3921-27del	XP_016866592.1:n.3921-29_3921-27del
XM_017011104.1:c.3891-29_3891-27del	XP_016866593.1:n.3891-29_3891-27del
XM_017011105.2:c.3861-29_3861-27del	XP_016866594.1:n.3861-29_3861-27del
XM_017011106.2:c.3732-29_3732-27del	XP_016866595.1:n.3732-29_3732-27del
XM_017011107.2:c.3711-29_3711-27del	XP_016866596.1:n.3711-29_3711-27del
XR_002956289.1:n.4103-29_4103-27del
NM_001363725.2:c.1560-29_1560-27del	NP_001350654.1:n.1560-29_1560-27del
NM_001371656.1:c.3939-29_3939-27del	NP_001358585.1:n.3939-29_3939-27del
NM_001374820.1:c.3939-29_3939-27del	NP_001361749.1:n.3939-29_3939-27del
NM_001374828.1:c.4059-29_4059-27del MANE Select	NP_001361757.1:n.4059-29_4059-27del
NM_017519.3:c.3900-29_3900-27del	NP_059989.3:n.3900-29_3900-27del