Canonical Allele Identifier: CA1096290062

Gene: ARID1B

Linked Data

• dbSNP Id: rs1793244024
• gnomAD v3: 6-157190027-CCT-C
• gnomAD v4: 6-157190027-CCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190032_157190033del , CM000668.2:g.157190032_157190033del	GRCh38
NC_000006.11:g.157511166_157511167del , CM000668.1:g.157511166_157511167del	GRCh37
NC_000006.10:g.157552858_157552859del	NCBI36
NG_032093.1:g.417103_417104del
NG_032093.2:g.417103_417104del
NG_066624.1:g.419007_419008del

Transcript Alleles

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