Canonical Allele Identifier: CA366241317

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4579A>C	ENSP00000055163.8:p.Ser1527Arg
ENST00000414678.8:c.4648A>C	ENSP00000412835.3:p.Ser1550Arg
ENST00000637015.2:c.4867A>C	ENSP00000489729.2:p.Ser1623Arg
ENST00000346085.10:c.4618A>C	ENSP00000344546.5:p.Ser1540Arg
ENST00000350026.10:c.4330A>C	ENSP00000055163.7:p.Ser1444Arg
ENST00000414678.7:c.2896A>C	ENSP00000412835.2:p.Ser966Arg
ENST00000635849.1:c.2059A>C	ENSP00000490948.1:p.Ser687Arg
ENST00000635957.1:c.1690A>C	ENSP00000490385.1:p.Ser564Arg
ENST00000636227.1:n.3201A>C
ENST00000636254.1:n.658A>C
ENST00000636930.2:c.4738A>C MANE Select	ENSP00000490491.2:p.Ser1580Arg
ENST00000636940.1:n.2735A>C
ENST00000637015.1:c.2106A>C
ENST00000637568.1:c.2020A>C
ENST00000637741.1:n.1404A>C
ENST00000637810.1:c.2080A>C	ENSP00000489636.1:p.Ser694Arg
ENST00000637904.1:c.2239A>C	ENSP00000490550.1:p.Ser747Arg
ENST00000647938.1:c.4369A>C	ENSP00000498155.1:p.Ser1457Arg
ENST00000346085.9:c.4369A>C	ENSP00000344546.4:p.Ser1457Arg
ENST00000350026.9:c.4330A>C	ENSP00000055163.7:p.Ser1444Arg
ENST00000414678.6:c.2896A>C	ENSP00000412835.2:p.Ser966Arg
NM_017519.2:c.4330A>C	NP_059989.2:p.Ser1444Arg
NM_020732.3:c.4369A>C	NP_065783.3:p.Ser1457Arg
XM_005267069.3:c.4489A>C	XP_005267126.2:p.Ser1497Arg
XM_011535984.1:c.3568A>C	XP_011534286.1:p.Ser1190Arg
XM_011535985.1:c.3388A>C	XP_011534287.1:p.Ser1130Arg
XM_011535986.1:c.3148A>C	XP_011534288.1:p.Ser1050Arg
XM_011535987.1:c.2767A>C	XP_011534289.1:p.Ser923Arg
XM_011535988.1:c.1630A>C	XP_011534290.1:p.Ser544Arg
NM_001346813.1:c.4489A>C	NP_001333742.1:p.Ser1497Arg
NM_001363725.1:c.2239A>C	NP_001350654.1:p.Ser747Arg
XM_011535984.2:c.4699A>C	XP_011534286.2:p.Ser1567Arg
XM_011535988.3:c.1630A>C	XP_011534290.1:p.Ser544Arg
XM_017011103.2:c.4600A>C	XP_016866592.1:p.Ser1534Arg
XM_017011104.1:c.4570A>C	XP_016866593.1:p.Ser1524Arg
XM_017011105.2:c.4540A>C	XP_016866594.1:p.Ser1514Arg
XM_017011106.2:c.4411A>C	XP_016866595.1:p.Ser1471Arg
XM_017011107.2:c.4390A>C	XP_016866596.1:p.Ser1464Arg
XR_002956289.1:n.4685A>C
NM_001363725.2:c.2239A>C	NP_001350654.1:p.Ser747Arg
NM_001371656.1:c.4618A>C	NP_001358585.1:p.Ser1540Arg
NM_001374820.1:c.4618A>C	NP_001361749.1:p.Ser1540Arg
NM_001374828.1:c.4738A>C MANE Select	NP_001361757.1:p.Ser1580Arg
NM_017519.3:c.4579A>C	NP_059989.3:p.Ser1527Arg