Canonical Allele Identifier: CA366241320

Gene: ARID1B

Linked Data

• dbSNP Id: rs1305457851
• gnomAD v4: 6-157200964-G-A
• MyVariant Identifiers: chr6:g.157522098G>A (hg19) ; chr6:g.157200964G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200964G>A , CM000668.2:g.157200964G>A	GRCh38
NC_000006.11:g.157522098G>A , CM000668.1:g.157522098G>A	GRCh37
NC_000006.10:g.157563790G>A	NCBI36
NG_032093.1:g.428035G>A
NG_032093.2:g.428035G>A
NG_066624.1:g.429939G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4580G>A	ENSP00000055163.8:p.Ser1527Asn
ENST00000414678.8:c.4649G>A	ENSP00000412835.3:p.Ser1550Asn
ENST00000637015.2:c.4868G>A	ENSP00000489729.2:p.Ser1623Asn
ENST00000346085.10:c.4619G>A	ENSP00000344546.5:p.Ser1540Asn
ENST00000350026.10:c.4331G>A	ENSP00000055163.7:p.Ser1444Asn
ENST00000414678.7:c.2897G>A	ENSP00000412835.2:p.Ser966Asn
ENST00000635849.1:c.2060G>A	ENSP00000490948.1:p.Ser687Asn
ENST00000635957.1:c.1691G>A	ENSP00000490385.1:p.Ser564Asn
ENST00000636227.1:n.3202G>A
ENST00000636254.1:n.659G>A
ENST00000636930.2:c.4739G>A MANE Select	ENSP00000490491.2:p.Ser1580Asn
ENST00000636940.1:n.2736G>A
ENST00000637015.1:c.2107G>A
ENST00000637568.1:c.2021G>A
ENST00000637741.1:n.1405G>A
ENST00000637810.1:c.2081G>A	ENSP00000489636.1:p.Ser694Asn
ENST00000637904.1:c.2240G>A	ENSP00000490550.1:p.Ser747Asn
ENST00000647938.1:c.4370G>A	ENSP00000498155.1:p.Ser1457Asn
ENST00000346085.9:c.4370G>A	ENSP00000344546.4:p.Ser1457Asn
ENST00000350026.9:c.4331G>A	ENSP00000055163.7:p.Ser1444Asn
ENST00000414678.6:c.2897G>A	ENSP00000412835.2:p.Ser966Asn
NM_017519.2:c.4331G>A	NP_059989.2:p.Ser1444Asn
NM_020732.3:c.4370G>A	NP_065783.3:p.Ser1457Asn
XM_005267069.3:c.4490G>A	XP_005267126.2:p.Ser1497Asn
XM_011535984.1:c.3569G>A	XP_011534286.1:p.Ser1190Asn
XM_011535985.1:c.3389G>A	XP_011534287.1:p.Ser1130Asn
XM_011535986.1:c.3149G>A	XP_011534288.1:p.Ser1050Asn
XM_011535987.1:c.2768G>A	XP_011534289.1:p.Ser923Asn
XM_011535988.1:c.1631G>A	XP_011534290.1:p.Ser544Asn
NM_001346813.1:c.4490G>A	NP_001333742.1:p.Ser1497Asn
NM_001363725.1:c.2240G>A	NP_001350654.1:p.Ser747Asn
XM_011535984.2:c.4700G>A	XP_011534286.2:p.Ser1567Asn
XM_011535988.3:c.1631G>A	XP_011534290.1:p.Ser544Asn
XM_017011103.2:c.4601G>A	XP_016866592.1:p.Ser1534Asn
XM_017011104.1:c.4571G>A	XP_016866593.1:p.Ser1524Asn
XM_017011105.2:c.4541G>A	XP_016866594.1:p.Ser1514Asn
XM_017011106.2:c.4412G>A	XP_016866595.1:p.Ser1471Asn
XM_017011107.2:c.4391G>A	XP_016866596.1:p.Ser1464Asn
XR_002956289.1:n.4686G>A
NM_001363725.2:c.2240G>A	NP_001350654.1:p.Ser747Asn
NM_001371656.1:c.4619G>A	NP_001358585.1:p.Ser1540Asn
NM_001374820.1:c.4619G>A	NP_001361749.1:p.Ser1540Asn
NM_001374828.1:c.4739G>A MANE Select	NP_001361757.1:p.Ser1580Asn
NM_017519.3:c.4580G>A	NP_059989.3:p.Ser1527Asn