Canonical Allele Identifier: CA452784837

Gene: ARID1B

Linked Data

• dbSNP Id: rs1197819486
• gnomAD v3: 6-157201397-A-C
• gnomAD v4: 6-157201397-A-C
• MyVariant Identifiers: chr6:g.157522531A>C (hg19) ; chr6:g.157201397A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201397A>C , CM000668.2:g.157201397A>C	GRCh38
NC_000006.11:g.157522531A>C , CM000668.1:g.157522531A>C	GRCh37
NC_000006.10:g.157564223A>C	NCBI36
NG_032093.1:g.428468A>C
NG_032093.2:g.428468A>C
NG_066624.1:g.430372A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.5013A>C	ENSP00000055163.8:p.Pro1671=
ENST00000414678.8:c.5082A>C	ENSP00000412835.3:p.Pro1694=
ENST00000637015.2:c.5301A>C	ENSP00000489729.2:p.Pro1767=
ENST00000346085.10:c.5052A>C	ENSP00000344546.5:p.Pro1684=
ENST00000350026.10:c.4764A>C	ENSP00000055163.7:p.Pro1588=
ENST00000414678.7:c.3330A>C	ENSP00000412835.2:p.Pro1110=
ENST00000635849.1:c.2493A>C	ENSP00000490948.1:p.Pro831=
ENST00000635957.1:c.2124A>C	ENSP00000490385.1:p.Pro708=
ENST00000636227.1:n.3635A>C
ENST00000636254.1:n.1092A>C
ENST00000636930.2:c.5172A>C MANE Select	ENSP00000490491.2:p.Pro1724=
ENST00000636940.1:n.3169A>C
ENST00000637015.1:c.2540A>C
ENST00000637568.1:c.2454A>C
ENST00000637741.1:n.1838A>C
ENST00000637810.1:c.2514A>C	ENSP00000489636.1:p.Pro838=
ENST00000637904.1:c.2673A>C	ENSP00000490550.1:p.Pro891=
ENST00000647938.1:c.4803A>C	ENSP00000498155.1:p.Pro1601=
ENST00000346085.9:c.4803A>C	ENSP00000344546.4:p.Pro1601=
ENST00000350026.9:c.4764A>C	ENSP00000055163.7:p.Pro1588=
ENST00000414678.6:c.3330A>C	ENSP00000412835.2:p.Pro1110=
NM_017519.2:c.4764A>C	NP_059989.2:p.Pro1588=
NM_020732.3:c.4803A>C	NP_065783.3:p.Pro1601=
XM_005267069.3:c.4923A>C	XP_005267126.2:p.Pro1641=
XM_011535984.1:c.4002A>C	XP_011534286.1:p.Pro1334=
XM_011535985.1:c.3822A>C	XP_011534287.1:p.Pro1274=
XM_011535986.1:c.3582A>C	XP_011534288.1:p.Pro1194=
XM_011535987.1:c.3201A>C	XP_011534289.1:p.Pro1067=
XM_011535988.1:c.2064A>C	XP_011534290.1:p.Pro688=
NM_001346813.1:c.4923A>C	NP_001333742.1:p.Pro1641=
NM_001363725.1:c.2673A>C	NP_001350654.1:p.Pro891=
XM_011535984.2:c.5133A>C	XP_011534286.2:p.Pro1711=
XM_011535988.3:c.2064A>C	XP_011534290.1:p.Pro688=
XM_017011103.2:c.5034A>C	XP_016866592.1:p.Pro1678=
XM_017011104.1:c.5004A>C	XP_016866593.1:p.Pro1668=
XM_017011105.2:c.4974A>C	XP_016866594.1:p.Pro1658=
XM_017011106.2:c.4845A>C	XP_016866595.1:p.Pro1615=
XM_017011107.2:c.4824A>C	XP_016866596.1:p.Pro1608=
XR_002956289.1:n.5119A>C
NM_001363725.2:c.2673A>C	NP_001350654.1:p.Pro891=
NM_001371656.1:c.5052A>C	NP_001358585.1:p.Pro1684=
NM_001374820.1:c.5052A>C	NP_001361749.1:p.Pro1684=
NM_001374828.1:c.5172A>C MANE Select	NP_001361757.1:p.Pro1724=
NM_017519.3:c.5013A>C	NP_059989.3:p.Pro1671=