Canonical Allele Identifier: CA452978048

Gene: ARID1B

Linked Data

• dbSNP Id: rs1180916109
• gnomAD v2: 6-157505448-G-A
• gnomAD v4: 6-157184314-G-A
• COSMIC: COSM5422317 ; COSM5422318
• MyVariant Identifiers: chr6:g.157505448G>A (hg19) ; chr6:g.157184314G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157184314G>A , CM000668.2:g.157184314G>A	GRCh38
NC_000006.11:g.157505448G>A , CM000668.1:g.157505448G>A	GRCh37
NC_000006.10:g.157547140G>A	NCBI36
NG_032093.1:g.411385G>A
NG_032093.2:g.411385G>A
NG_066624.1:g.413289G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3639G>A	ENSP00000055163.8:p.Lys1213=
ENST00000414678.8:c.3708G>A	ENSP00000412835.3:p.Lys1236=
ENST00000637015.2:c.3927G>A	ENSP00000489729.2:p.Lys1309=
ENST00000319584.11:c.1812G>A	ENSP00000313006.7:p.Lys604=
ENST00000346085.10:c.3678G>A	ENSP00000344546.5:p.Lys1226=
ENST00000350026.10:c.3390G>A	ENSP00000055163.7:p.Lys1130=
ENST00000414678.7:c.1956G>A	ENSP00000412835.2:p.Lys652=
ENST00000635849.1:c.1119G>A	ENSP00000490948.1:p.Lys373=
ENST00000635957.1:c.753G>A	ENSP00000490385.1:p.Lys251=
ENST00000636930.2:c.3798G>A MANE Select	ENSP00000490491.2:p.Lys1266=
ENST00000636940.1:n.1795G>A
ENST00000637015.1:c.1166G>A
ENST00000637568.1:c.1080G>A
ENST00000637741.1:n.464G>A
ENST00000637810.1:c.1140G>A	ENSP00000489636.1:p.Lys380=
ENST00000637904.1:c.1299G>A	ENSP00000490550.1:p.Lys433=
ENST00000647938.1:c.3429G>A	ENSP00000498155.1:p.Lys1143=
ENST00000319584.10:c.1815G>A	ENSP00000313006.6:p.Lys605=
ENST00000346085.9:c.3429G>A	ENSP00000344546.4:p.Lys1143=
ENST00000350026.9:c.3390G>A	ENSP00000055163.7:p.Lys1130=
ENST00000400790.3:c.591G>A	ENSP00000383596.3:p.Lys197=
ENST00000414678.6:c.1956G>A	ENSP00000412835.2:p.Lys652=
NM_017519.2:c.3390G>A	NP_059989.2:p.Lys1130=
NM_020732.3:c.3429G>A	NP_065783.3:p.Lys1143=
XM_005267069.3:c.3549G>A	XP_005267126.2:p.Lys1183=
XM_011535984.1:c.2628G>A	XP_011534286.1:p.Lys876=
XM_011535985.1:c.2448G>A	XP_011534287.1:p.Lys816=
XM_011535986.1:c.2208G>A	XP_011534288.1:p.Lys736=
XM_011535987.1:c.1827G>A	XP_011534289.1:p.Lys609=
XM_011535988.1:c.690G>A	XP_011534290.1:p.Lys230=
NM_001346813.1:c.3549G>A	NP_001333742.1:p.Lys1183=
NM_001363725.1:c.1299G>A	NP_001350654.1:p.Lys433=
XM_011535984.2:c.3759G>A	XP_011534286.2:p.Lys1253=
XM_011535988.3:c.690G>A	XP_011534290.1:p.Lys230=
XM_017011103.2:c.3660G>A	XP_016866592.1:p.Lys1220=
XM_017011104.1:c.3630G>A	XP_016866593.1:p.Lys1210=
XM_017011105.2:c.3600G>A	XP_016866594.1:p.Lys1200=
XM_017011106.2:c.3471G>A	XP_016866595.1:p.Lys1157=
XM_017011107.2:c.3450G>A	XP_016866596.1:p.Lys1150=
XR_002956289.1:n.3842G>A
NM_001363725.2:c.1299G>A	NP_001350654.1:p.Lys433=
NM_001371656.1:c.3678G>A	NP_001358585.1:p.Lys1226=
NM_001374820.1:c.3678G>A	NP_001361749.1:p.Lys1226=
NM_001374828.1:c.3798G>A MANE Select	NP_001361757.1:p.Lys1266=
NM_017519.3:c.3639G>A	NP_059989.3:p.Lys1213=