Canonical Allele Identifier: CA452783953

Gene: ARID1B

Linked Data

• dbSNP Id: rs1337744788
• gnomAD v2: 6-157519999-G-A
• gnomAD v4: 6-157198865-G-A
• MyVariant Identifiers: chr6:g.157519999G>A (hg19) ; chr6:g.157198865G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157198865G>A , CM000668.2:g.157198865G>A	GRCh38
NC_000006.11:g.157519999G>A , CM000668.1:g.157519999G>A	GRCh37
NC_000006.10:g.157561691G>A	NCBI36
NG_032093.1:g.425936G>A
NG_032093.2:g.425936G>A
NG_066624.1:g.427840G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4278G>A	ENSP00000055163.8:p.Pro1426=
ENST00000414678.8:c.4347G>A	ENSP00000412835.3:p.Pro1449=
ENST00000637015.2:c.4566G>A	ENSP00000489729.2:p.Pro1522=
ENST00000346085.10:c.4317G>A	ENSP00000344546.5:p.Pro1439=
ENST00000350026.10:c.4029G>A	ENSP00000055163.7:p.Pro1343=
ENST00000414678.7:c.2595G>A	ENSP00000412835.2:p.Pro865=
ENST00000635849.1:c.1758G>A	ENSP00000490948.1:p.Pro586=
ENST00000635957.1:c.1389G>A	ENSP00000490385.1:p.Pro463=
ENST00000636227.1:n.2900G>A
ENST00000636254.1:n.357G>A
ENST00000636930.2:c.4437G>A MANE Select	ENSP00000490491.2:p.Pro1479=
ENST00000636940.1:n.2434G>A
ENST00000637015.1:c.1805G>A
ENST00000637568.1:c.1719G>A
ENST00000637741.1:n.1103G>A
ENST00000637810.1:c.1779G>A	ENSP00000489636.1:p.Pro593=
ENST00000637904.1:c.1938G>A	ENSP00000490550.1:p.Pro646=
ENST00000647938.1:c.4068G>A	ENSP00000498155.1:p.Pro1356=
ENST00000346085.9:c.4068G>A	ENSP00000344546.4:p.Pro1356=
ENST00000350026.9:c.4029G>A	ENSP00000055163.7:p.Pro1343=
ENST00000414678.6:c.2595G>A	ENSP00000412835.2:p.Pro865=
NM_017519.2:c.4029G>A	NP_059989.2:p.Pro1343=
NM_020732.3:c.4068G>A	NP_065783.3:p.Pro1356=
XM_005267069.3:c.4188G>A	XP_005267126.2:p.Pro1396=
XM_011535984.1:c.3267G>A	XP_011534286.1:p.Pro1089=
XM_011535985.1:c.3087G>A	XP_011534287.1:p.Pro1029=
XM_011535986.1:c.2847G>A	XP_011534288.1:p.Pro949=
XM_011535987.1:c.2466G>A	XP_011534289.1:p.Pro822=
XM_011535988.1:c.1329G>A	XP_011534290.1:p.Pro443=
NM_001346813.1:c.4188G>A	NP_001333742.1:p.Pro1396=
NM_001363725.1:c.1938G>A	NP_001350654.1:p.Pro646=
XM_011535984.2:c.4398G>A	XP_011534286.2:p.Pro1466=
XM_011535988.3:c.1329G>A	XP_011534290.1:p.Pro443=
XM_017011103.2:c.4299G>A	XP_016866592.1:p.Pro1433=
XM_017011104.1:c.4269G>A	XP_016866593.1:p.Pro1423=
XM_017011105.2:c.4239G>A	XP_016866594.1:p.Pro1413=
XM_017011106.2:c.4110G>A	XP_016866595.1:p.Pro1370=
XM_017011107.2:c.4089G>A	XP_016866596.1:p.Pro1363=
XR_002956289.1:n.4427-1840G>A
NM_001363725.2:c.1938G>A	NP_001350654.1:p.Pro646=
NM_001371656.1:c.4317G>A	NP_001358585.1:p.Pro1439=
NM_001374820.1:c.4317G>A	NP_001361749.1:p.Pro1439=
NM_001374828.1:c.4437G>A MANE Select	NP_001361757.1:p.Pro1479=
NM_017519.3:c.4278G>A	NP_059989.3:p.Pro1426=