Canonical Allele Identifier: CA366242672

Gene: ARID1B

Linked Data

• dbSNP Id: rs1168651010
• gnomAD v2: 6-157522481-C-A
• gnomAD v4: 6-157201347-C-A
• MyVariant Identifiers: chr6:g.157522481C>A (hg19) ; chr6:g.157201347C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201347C>A , CM000668.2:g.157201347C>A	GRCh38
NC_000006.11:g.157522481C>A , CM000668.1:g.157522481C>A	GRCh37
NC_000006.10:g.157564173C>A	NCBI36
NG_032093.1:g.428418C>A
NG_032093.2:g.428418C>A
NG_066624.1:g.430322C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4963C>A	ENSP00000055163.8:p.Pro1655Thr
ENST00000414678.8:c.5032C>A	ENSP00000412835.3:p.Pro1678Thr
ENST00000637015.2:c.5251C>A	ENSP00000489729.2:p.Pro1751Thr
ENST00000346085.10:c.5002C>A	ENSP00000344546.5:p.Pro1668Thr
ENST00000350026.10:c.4714C>A	ENSP00000055163.7:p.Pro1572Thr
ENST00000414678.7:c.3280C>A	ENSP00000412835.2:p.Pro1094Thr
ENST00000635849.1:c.2443C>A	ENSP00000490948.1:p.Pro815Thr
ENST00000635957.1:c.2074C>A	ENSP00000490385.1:p.Pro692Thr
ENST00000636227.1:n.3585C>A
ENST00000636254.1:n.1042C>A
ENST00000636930.2:c.5122C>A MANE Select	ENSP00000490491.2:p.Pro1708Thr
ENST00000636940.1:n.3119C>A
ENST00000637015.1:c.2490C>A
ENST00000637568.1:c.2404C>A
ENST00000637741.1:n.1788C>A
ENST00000637810.1:c.2464C>A	ENSP00000489636.1:p.Pro822Thr
ENST00000637904.1:c.2623C>A	ENSP00000490550.1:p.Pro875Thr
ENST00000647938.1:c.4753C>A	ENSP00000498155.1:p.Pro1585Thr
ENST00000346085.9:c.4753C>A	ENSP00000344546.4:p.Pro1585Thr
ENST00000350026.9:c.4714C>A	ENSP00000055163.7:p.Pro1572Thr
ENST00000414678.6:c.3280C>A	ENSP00000412835.2:p.Pro1094Thr
NM_017519.2:c.4714C>A	NP_059989.2:p.Pro1572Thr
NM_020732.3:c.4753C>A	NP_065783.3:p.Pro1585Thr
XM_005267069.3:c.4873C>A	XP_005267126.2:p.Pro1625Thr
XM_011535984.1:c.3952C>A	XP_011534286.1:p.Pro1318Thr
XM_011535985.1:c.3772C>A	XP_011534287.1:p.Pro1258Thr
XM_011535986.1:c.3532C>A	XP_011534288.1:p.Pro1178Thr
XM_011535987.1:c.3151C>A	XP_011534289.1:p.Pro1051Thr
XM_011535988.1:c.2014C>A	XP_011534290.1:p.Pro672Thr
NM_001346813.1:c.4873C>A	NP_001333742.1:p.Pro1625Thr
NM_001363725.1:c.2623C>A	NP_001350654.1:p.Pro875Thr
XM_011535984.2:c.5083C>A	XP_011534286.2:p.Pro1695Thr
XM_011535988.3:c.2014C>A	XP_011534290.1:p.Pro672Thr
XM_017011103.2:c.4984C>A	XP_016866592.1:p.Pro1662Thr
XM_017011104.1:c.4954C>A	XP_016866593.1:p.Pro1652Thr
XM_017011105.2:c.4924C>A	XP_016866594.1:p.Pro1642Thr
XM_017011106.2:c.4795C>A	XP_016866595.1:p.Pro1599Thr
XM_017011107.2:c.4774C>A	XP_016866596.1:p.Pro1592Thr
XR_002956289.1:n.5069C>A
NM_001363725.2:c.2623C>A	NP_001350654.1:p.Pro875Thr
NM_001371656.1:c.5002C>A	NP_001358585.1:p.Pro1668Thr
NM_001374820.1:c.5002C>A	NP_001361749.1:p.Pro1668Thr
NM_001374828.1:c.5122C>A MANE Select	NP_001361757.1:p.Pro1708Thr
NM_017519.3:c.4963C>A	NP_059989.3:p.Pro1655Thr