Canonical Allele Identifier: CA366241321

Gene: ARID1B

Linked Data

• dbSNP Id: rs1305457851
• gnomAD v2: 6-157522098-G-C
• gnomAD v4: 6-157200964-G-C
• MyVariant Identifiers: chr6:g.157522098G>C (hg19) ; chr6:g.157200964G>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4580G>C	ENSP00000055163.8:p.Ser1527Thr
ENST00000414678.8:c.4649G>C	ENSP00000412835.3:p.Ser1550Thr
ENST00000637015.2:c.4868G>C	ENSP00000489729.2:p.Ser1623Thr
ENST00000346085.10:c.4619G>C	ENSP00000344546.5:p.Ser1540Thr
ENST00000350026.10:c.4331G>C	ENSP00000055163.7:p.Ser1444Thr
ENST00000414678.7:c.2897G>C	ENSP00000412835.2:p.Ser966Thr
ENST00000635849.1:c.2060G>C	ENSP00000490948.1:p.Ser687Thr
ENST00000635957.1:c.1691G>C	ENSP00000490385.1:p.Ser564Thr
ENST00000636227.1:n.3202G>C
ENST00000636254.1:n.659G>C
ENST00000636930.2:c.4739G>C MANE Select	ENSP00000490491.2:p.Ser1580Thr
ENST00000636940.1:n.2736G>C
ENST00000637015.1:c.2107G>C
ENST00000637568.1:c.2021G>C
ENST00000637741.1:n.1405G>C
ENST00000637810.1:c.2081G>C	ENSP00000489636.1:p.Ser694Thr
ENST00000637904.1:c.2240G>C	ENSP00000490550.1:p.Ser747Thr
ENST00000647938.1:c.4370G>C	ENSP00000498155.1:p.Ser1457Thr
ENST00000346085.9:c.4370G>C	ENSP00000344546.4:p.Ser1457Thr
ENST00000350026.9:c.4331G>C	ENSP00000055163.7:p.Ser1444Thr
ENST00000414678.6:c.2897G>C	ENSP00000412835.2:p.Ser966Thr
NM_017519.2:c.4331G>C	NP_059989.2:p.Ser1444Thr
NM_020732.3:c.4370G>C	NP_065783.3:p.Ser1457Thr
XM_005267069.3:c.4490G>C	XP_005267126.2:p.Ser1497Thr
XM_011535984.1:c.3569G>C	XP_011534286.1:p.Ser1190Thr
XM_011535985.1:c.3389G>C	XP_011534287.1:p.Ser1130Thr
XM_011535986.1:c.3149G>C	XP_011534288.1:p.Ser1050Thr
XM_011535987.1:c.2768G>C	XP_011534289.1:p.Ser923Thr
XM_011535988.1:c.1631G>C	XP_011534290.1:p.Ser544Thr
NM_001346813.1:c.4490G>C	NP_001333742.1:p.Ser1497Thr
NM_001363725.1:c.2240G>C	NP_001350654.1:p.Ser747Thr
XM_011535984.2:c.4700G>C	XP_011534286.2:p.Ser1567Thr
XM_011535988.3:c.1631G>C	XP_011534290.1:p.Ser544Thr
XM_017011103.2:c.4601G>C	XP_016866592.1:p.Ser1534Thr
XM_017011104.1:c.4571G>C	XP_016866593.1:p.Ser1524Thr
XM_017011105.2:c.4541G>C	XP_016866594.1:p.Ser1514Thr
XM_017011106.2:c.4412G>C	XP_016866595.1:p.Ser1471Thr
XM_017011107.2:c.4391G>C	XP_016866596.1:p.Ser1464Thr
XR_002956289.1:n.4686G>C
NM_001363725.2:c.2240G>C	NP_001350654.1:p.Ser747Thr
NM_001371656.1:c.4619G>C	NP_001358585.1:p.Ser1540Thr
NM_001374820.1:c.4619G>C	NP_001361749.1:p.Ser1540Thr
NM_001374828.1:c.4739G>C MANE Select	NP_001361757.1:p.Ser1580Thr
NM_017519.3:c.4580G>C	NP_059989.3:p.Ser1527Thr