Canonical Allele Identifier: CA4067767

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 1695172
• ClinVar RCV Id: RCV002263422
• dbSNP Id: rs745670548
• ExAC: 6:157522507 C / T
• gnomAD v2: 6-157522507-C-T
• gnomAD v3: 6-157201373-C-T
• gnomAD v4: 6-157201373-C-T
• COSMIC: COSM3410734 ; COSM3410735
• MyVariant Identifiers: chr6:g.157522507C>T (hg19) ; chr6:g.157201373C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201373C>T , CM000668.2:g.157201373C>T	GRCh38
NC_000006.11:g.157522507C>T , CM000668.1:g.157522507C>T	GRCh37
NC_000006.10:g.157564199C>T	NCBI36
NG_032093.1:g.428444C>T
NG_032093.2:g.428444C>T
NG_066624.1:g.430348C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4989C>T	ENSP00000055163.8:p.Thr1663=
ENST00000414678.8:c.5058C>T	ENSP00000412835.3:p.Thr1686=
ENST00000637015.2:c.5277C>T	ENSP00000489729.2:p.Thr1759=
ENST00000346085.10:c.5028C>T	ENSP00000344546.5:p.Thr1676=
ENST00000350026.10:c.4740C>T	ENSP00000055163.7:p.Thr1580=
ENST00000414678.7:c.3306C>T	ENSP00000412835.2:p.Thr1102=
ENST00000635849.1:c.2469C>T	ENSP00000490948.1:p.Thr823=
ENST00000635957.1:c.2100C>T	ENSP00000490385.1:p.Thr700=
ENST00000636227.1:n.3611C>T
ENST00000636254.1:n.1068C>T
ENST00000636930.2:c.5148C>T MANE Select	ENSP00000490491.2:p.Thr1716=
ENST00000636940.1:n.3145C>T
ENST00000637015.1:c.2516C>T
ENST00000637568.1:c.2430C>T
ENST00000637741.1:n.1814C>T
ENST00000637810.1:c.2490C>T	ENSP00000489636.1:p.Thr830=
ENST00000637904.1:c.2649C>T	ENSP00000490550.1:p.Thr883=
ENST00000647938.1:c.4779C>T	ENSP00000498155.1:p.Thr1593=
ENST00000346085.9:c.4779C>T	ENSP00000344546.4:p.Thr1593=
ENST00000350026.9:c.4740C>T	ENSP00000055163.7:p.Thr1580=
ENST00000414678.6:c.3306C>T	ENSP00000412835.2:p.Thr1102=
NM_017519.2:c.4740C>T	NP_059989.2:p.Thr1580=
NM_020732.3:c.4779C>T	NP_065783.3:p.Thr1593=
XM_005267069.3:c.4899C>T	XP_005267126.2:p.Thr1633=
XM_011535984.1:c.3978C>T	XP_011534286.1:p.Thr1326=
XM_011535985.1:c.3798C>T	XP_011534287.1:p.Thr1266=
XM_011535986.1:c.3558C>T	XP_011534288.1:p.Thr1186=
XM_011535987.1:c.3177C>T	XP_011534289.1:p.Thr1059=
XM_011535988.1:c.2040C>T	XP_011534290.1:p.Thr680=
NM_001346813.1:c.4899C>T	NP_001333742.1:p.Thr1633=
NM_001363725.1:c.2649C>T	NP_001350654.1:p.Thr883=
XM_011535984.2:c.5109C>T	XP_011534286.2:p.Thr1703=
XM_011535988.3:c.2040C>T	XP_011534290.1:p.Thr680=
XM_017011103.2:c.5010C>T	XP_016866592.1:p.Thr1670=
XM_017011104.1:c.4980C>T	XP_016866593.1:p.Thr1660=
XM_017011105.2:c.4950C>T	XP_016866594.1:p.Thr1650=
XM_017011106.2:c.4821C>T	XP_016866595.1:p.Thr1607=
XM_017011107.2:c.4800C>T	XP_016866596.1:p.Thr1600=
XR_002956289.1:n.5095C>T
NM_001363725.2:c.2649C>T	NP_001350654.1:p.Thr883=
NM_001371656.1:c.5028C>T	NP_001358585.1:p.Thr1676=
NM_001374820.1:c.5028C>T	NP_001361749.1:p.Thr1676=
NM_001374828.1:c.5148C>T MANE Select	NP_001361757.1:p.Thr1716=
NM_017519.3:c.4989C>T	NP_059989.3:p.Thr1663=