Canonical Allele Identifier: CA452780747

Gene: ARID1B

Linked Data

• dbSNP Id: rs1459507646
• gnomAD v2: 6-157502159-G-C
• gnomAD v3: 6-157181025-G-C
• gnomAD v4: 6-157181025-G-C
• MyVariant Identifiers: chr6:g.157502159G>C (hg19) ; chr6:g.157181025G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181025G>C , CM000668.2:g.157181025G>C	GRCh38
NC_000006.11:g.157502159G>C , CM000668.1:g.157502159G>C	GRCh37
NC_000006.10:g.157543851G>C	NCBI36
NG_032093.1:g.408096G>C
NG_032093.2:g.408096G>C
NG_066624.1:g.410000G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3402G>C	ENSP00000055163.8:p.Gly1134=
ENST00000414678.8:c.3471G>C	ENSP00000412835.3:p.Gly1157=
ENST00000637015.2:c.3690G>C	ENSP00000489729.2:p.Gly1230=
ENST00000319584.11:c.1575G>C	ENSP00000313006.7:p.Gly525=
ENST00000346085.10:c.3441G>C	ENSP00000344546.5:p.Gly1147=
ENST00000350026.10:c.3153G>C	ENSP00000055163.7:p.Gly1051=
ENST00000414678.7:c.1719G>C	ENSP00000412835.2:p.Gly573=
ENST00000635849.1:c.882G>C	ENSP00000490948.1:p.Gly294=
ENST00000635957.1:c.516G>C	ENSP00000490385.1:p.Gly172=
ENST00000636930.2:c.3561G>C MANE Select	ENSP00000490491.2:p.Gly1187=
ENST00000636940.1:n.1558G>C
ENST00000637015.1:c.929G>C
ENST00000637568.1:c.843G>C
ENST00000637741.1:n.227G>C
ENST00000637810.1:c.903G>C	ENSP00000489636.1:p.Gly301=
ENST00000637904.1:c.1062G>C	ENSP00000490550.1:p.Gly354=
ENST00000647938.1:c.3192G>C	ENSP00000498155.1:p.Gly1064=
ENST00000319584.10:c.1578G>C	ENSP00000313006.6:p.Gly526=
ENST00000346085.9:c.3192G>C	ENSP00000344546.4:p.Gly1064=
ENST00000350026.9:c.3153G>C	ENSP00000055163.7:p.Gly1051=
ENST00000400790.3:c.354G>C	ENSP00000383596.3:p.Gly118=
ENST00000414678.6:c.1719G>C	ENSP00000412835.2:p.Gly573=
ENST00000478761.3:c.763G>C
NM_017519.2:c.3153G>C	NP_059989.2:p.Gly1051=
NM_020732.3:c.3192G>C	NP_065783.3:p.Gly1064=
XM_005267069.3:c.3312G>C	XP_005267126.2:p.Gly1104=
XM_011535984.1:c.2391G>C	XP_011534286.1:p.Gly797=
XM_011535985.1:c.2211G>C	XP_011534287.1:p.Gly737=
XM_011535986.1:c.1971G>C	XP_011534288.1:p.Gly657=
XM_011535987.1:c.1590G>C	XP_011534289.1:p.Gly530=
XM_011535988.1:c.453G>C	XP_011534290.1:p.Gly151=
NM_001346813.1:c.3312G>C	NP_001333742.1:p.Gly1104=
NM_001363725.1:c.1062G>C	NP_001350654.1:p.Gly354=
XM_011535984.2:c.3522G>C	XP_011534286.2:p.Gly1174=
XM_011535988.3:c.453G>C	XP_011534290.1:p.Gly151=
XM_017011103.2:c.3423G>C	XP_016866592.1:p.Gly1141=
XM_017011104.1:c.3393G>C	XP_016866593.1:p.Gly1131=
XM_017011105.2:c.3363G>C	XP_016866594.1:p.Gly1121=
XM_017011106.2:c.3234G>C	XP_016866595.1:p.Gly1078=
XM_017011107.2:c.3213G>C	XP_016866596.1:p.Gly1071=
XR_002956289.1:n.3605G>C
NM_001363725.2:c.1062G>C	NP_001350654.1:p.Gly354=
NM_001371656.1:c.3441G>C	NP_001358585.1:p.Gly1147=
NM_001374820.1:c.3441G>C	NP_001361749.1:p.Gly1147=
NM_001374828.1:c.3561G>C MANE Select	NP_001361757.1:p.Gly1187=
NM_017519.3:c.3402G>C	NP_059989.3:p.Gly1134=