Canonical Allele Identifier: CA366234832

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157190060-G-T
• MyVariant Identifiers: chr6:g.157511194G>T (hg19) ; chr6:g.157190060G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190060G>T , CM000668.2:g.157190060G>T	GRCh38
NC_000006.11:g.157511194G>T , CM000668.1:g.157511194G>T	GRCh37
NC_000006.10:g.157552886G>T	NCBI36
NG_032093.1:g.417131G>T
NG_032093.2:g.417131G>T
NG_066624.1:g.419035G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3922G>T	ENSP00000055163.8:p.Asp1308Tyr
ENST00000414678.8:c.3991G>T	ENSP00000412835.3:p.Asp1331Tyr
ENST00000637015.2:c.4210G>T	ENSP00000489729.2:p.Asp1404Tyr
ENST00000346085.10:c.3961G>T	ENSP00000344546.5:p.Asp1321Tyr
ENST00000350026.10:c.3673G>T	ENSP00000055163.7:p.Asp1225Tyr
ENST00000414678.7:c.2239G>T	ENSP00000412835.2:p.Asp747Tyr
ENST00000635849.1:c.1402G>T	ENSP00000490948.1:p.Asp468Tyr
ENST00000635957.1:c.1033G>T	ENSP00000490385.1:p.Asp345Tyr
ENST00000636930.2:c.4081G>T MANE Select	ENSP00000490491.2:p.Asp1361Tyr
ENST00000636940.1:n.2078G>T
ENST00000637015.1:c.1449G>T
ENST00000637568.1:c.1363G>T
ENST00000637741.1:n.747G>T
ENST00000637810.1:c.1423G>T	ENSP00000489636.1:p.Asp475Tyr
ENST00000637904.1:c.1582G>T	ENSP00000490550.1:p.Asp528Tyr
ENST00000647938.1:c.3712G>T	ENSP00000498155.1:p.Asp1238Tyr
ENST00000346085.9:c.3712G>T	ENSP00000344546.4:p.Asp1238Tyr
ENST00000350026.9:c.3673G>T	ENSP00000055163.7:p.Asp1225Tyr
ENST00000414678.6:c.2239G>T	ENSP00000412835.2:p.Asp747Tyr
NM_017519.2:c.3673G>T	NP_059989.2:p.Asp1225Tyr
NM_020732.3:c.3712G>T	NP_065783.3:p.Asp1238Tyr
XM_005267069.3:c.3832G>T	XP_005267126.2:p.Asp1278Tyr
XM_011535984.1:c.2911G>T	XP_011534286.1:p.Asp971Tyr
XM_011535985.1:c.2731G>T	XP_011534287.1:p.Asp911Tyr
XM_011535986.1:c.2491G>T	XP_011534288.1:p.Asp831Tyr
XM_011535987.1:c.2110G>T	XP_011534289.1:p.Asp704Tyr
XM_011535988.1:c.973G>T	XP_011534290.1:p.Asp325Tyr
NM_001346813.1:c.3832G>T	NP_001333742.1:p.Asp1278Tyr
NM_001363725.1:c.1582G>T	NP_001350654.1:p.Asp528Tyr
XM_011535984.2:c.4042G>T	XP_011534286.2:p.Asp1348Tyr
XM_011535988.3:c.973G>T	XP_011534290.1:p.Asp325Tyr
XM_017011103.2:c.3943G>T	XP_016866592.1:p.Asp1315Tyr
XM_017011104.1:c.3913G>T	XP_016866593.1:p.Asp1305Tyr
XM_017011105.2:c.3883G>T	XP_016866594.1:p.Asp1295Tyr
XM_017011106.2:c.3754G>T	XP_016866595.1:p.Asp1252Tyr
XM_017011107.2:c.3733G>T	XP_016866596.1:p.Asp1245Tyr
XR_002956289.1:n.4125G>T
NM_001363725.2:c.1582G>T	NP_001350654.1:p.Asp528Tyr
NM_001371656.1:c.3961G>T	NP_001358585.1:p.Asp1321Tyr
NM_001374820.1:c.3961G>T	NP_001361749.1:p.Asp1321Tyr
NM_001374828.1:c.4081G>T MANE Select	NP_001361757.1:p.Asp1361Tyr
NM_017519.3:c.3922G>T	NP_059989.3:p.Asp1308Tyr