Canonical Allele Identifier: CA366241319

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522097A>T (hg19) ; chr6:g.157200963A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200963A>T , CM000668.2:g.157200963A>T	GRCh38
NC_000006.11:g.157522097A>T , CM000668.1:g.157522097A>T	GRCh37
NC_000006.10:g.157563789A>T	NCBI36
NG_032093.1:g.428034A>T
NG_032093.2:g.428034A>T
NG_066624.1:g.429938A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4579A>T	ENSP00000055163.8:p.Ser1527Cys
ENST00000414678.8:c.4648A>T	ENSP00000412835.3:p.Ser1550Cys
ENST00000637015.2:c.4867A>T	ENSP00000489729.2:p.Ser1623Cys
ENST00000346085.10:c.4618A>T	ENSP00000344546.5:p.Ser1540Cys
ENST00000350026.10:c.4330A>T	ENSP00000055163.7:p.Ser1444Cys
ENST00000414678.7:c.2896A>T	ENSP00000412835.2:p.Ser966Cys
ENST00000635849.1:c.2059A>T	ENSP00000490948.1:p.Ser687Cys
ENST00000635957.1:c.1690A>T	ENSP00000490385.1:p.Ser564Cys
ENST00000636227.1:n.3201A>T
ENST00000636254.1:n.658A>T
ENST00000636930.2:c.4738A>T MANE Select	ENSP00000490491.2:p.Ser1580Cys
ENST00000636940.1:n.2735A>T
ENST00000637015.1:c.2106A>T
ENST00000637568.1:c.2020A>T
ENST00000637741.1:n.1404A>T
ENST00000637810.1:c.2080A>T	ENSP00000489636.1:p.Ser694Cys
ENST00000637904.1:c.2239A>T	ENSP00000490550.1:p.Ser747Cys
ENST00000647938.1:c.4369A>T	ENSP00000498155.1:p.Ser1457Cys
ENST00000346085.9:c.4369A>T	ENSP00000344546.4:p.Ser1457Cys
ENST00000350026.9:c.4330A>T	ENSP00000055163.7:p.Ser1444Cys
ENST00000414678.6:c.2896A>T	ENSP00000412835.2:p.Ser966Cys
NM_017519.2:c.4330A>T	NP_059989.2:p.Ser1444Cys
NM_020732.3:c.4369A>T	NP_065783.3:p.Ser1457Cys
XM_005267069.3:c.4489A>T	XP_005267126.2:p.Ser1497Cys
XM_011535984.1:c.3568A>T	XP_011534286.1:p.Ser1190Cys
XM_011535985.1:c.3388A>T	XP_011534287.1:p.Ser1130Cys
XM_011535986.1:c.3148A>T	XP_011534288.1:p.Ser1050Cys
XM_011535987.1:c.2767A>T	XP_011534289.1:p.Ser923Cys
XM_011535988.1:c.1630A>T	XP_011534290.1:p.Ser544Cys
NM_001346813.1:c.4489A>T	NP_001333742.1:p.Ser1497Cys
NM_001363725.1:c.2239A>T	NP_001350654.1:p.Ser747Cys
XM_011535984.2:c.4699A>T	XP_011534286.2:p.Ser1567Cys
XM_011535988.3:c.1630A>T	XP_011534290.1:p.Ser544Cys
XM_017011103.2:c.4600A>T	XP_016866592.1:p.Ser1534Cys
XM_017011104.1:c.4570A>T	XP_016866593.1:p.Ser1524Cys
XM_017011105.2:c.4540A>T	XP_016866594.1:p.Ser1514Cys
XM_017011106.2:c.4411A>T	XP_016866595.1:p.Ser1471Cys
XM_017011107.2:c.4390A>T	XP_016866596.1:p.Ser1464Cys
XR_002956289.1:n.4685A>T
NM_001363725.2:c.2239A>T	NP_001350654.1:p.Ser747Cys
NM_001371656.1:c.4618A>T	NP_001358585.1:p.Ser1540Cys
NM_001374820.1:c.4618A>T	NP_001361749.1:p.Ser1540Cys
NM_001374828.1:c.4738A>T MANE Select	NP_001361757.1:p.Ser1580Cys
NM_017519.3:c.4579A>T	NP_059989.3:p.Ser1527Cys