Canonical Allele Identifier: CA452781603

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511217T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190083T>C , CM000668.2:g.157190083T>C	GRCh38
NC_000006.11:g.157511217T>C , CM000668.1:g.157511217T>C	GRCh37
NC_000006.10:g.157552909T>C	NCBI36
NG_032093.1:g.417154T>C
NG_032093.2:g.417154T>C
NG_066624.1:g.419058T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3945T>C	ENSP00000055163.8:p.Asp1315=
ENST00000414678.8:c.4014T>C	ENSP00000412835.3:p.Asp1338=
ENST00000637015.2:c.4233T>C	ENSP00000489729.2:p.Asp1411=
ENST00000346085.10:c.3984T>C	ENSP00000344546.5:p.Asp1328=
ENST00000350026.10:c.3696T>C	ENSP00000055163.7:p.Asp1232=
ENST00000414678.7:c.2262T>C	ENSP00000412835.2:p.Asp754=
ENST00000635849.1:c.1425T>C	ENSP00000490948.1:p.Asp475=
ENST00000635957.1:c.1056T>C	ENSP00000490385.1:p.Asp352=
ENST00000636930.2:c.4104T>C MANE Select	ENSP00000490491.2:p.Asp1368=
ENST00000636940.1:n.2101T>C
ENST00000637015.1:c.1472T>C
ENST00000637568.1:c.1386T>C
ENST00000637741.1:n.770T>C
ENST00000637810.1:c.1446T>C	ENSP00000489636.1:p.Asp482=
ENST00000637904.1:c.1605T>C	ENSP00000490550.1:p.Asp535=
ENST00000647938.1:c.3735T>C	ENSP00000498155.1:p.Asp1245=
ENST00000346085.9:c.3735T>C	ENSP00000344546.4:p.Asp1245=
ENST00000350026.9:c.3696T>C	ENSP00000055163.7:p.Asp1232=
ENST00000414678.6:c.2262T>C	ENSP00000412835.2:p.Asp754=
NM_017519.2:c.3696T>C	NP_059989.2:p.Asp1232=
NM_020732.3:c.3735T>C	NP_065783.3:p.Asp1245=
XM_005267069.3:c.3855T>C	XP_005267126.2:p.Asp1285=
XM_011535984.1:c.2934T>C	XP_011534286.1:p.Asp978=
XM_011535985.1:c.2754T>C	XP_011534287.1:p.Asp918=
XM_011535986.1:c.2514T>C	XP_011534288.1:p.Asp838=
XM_011535987.1:c.2133T>C	XP_011534289.1:p.Asp711=
XM_011535988.1:c.996T>C	XP_011534290.1:p.Asp332=
NM_001346813.1:c.3855T>C	NP_001333742.1:p.Asp1285=
NM_001363725.1:c.1605T>C	NP_001350654.1:p.Asp535=
XM_011535984.2:c.4065T>C	XP_011534286.2:p.Asp1355=
XM_011535988.3:c.996T>C	XP_011534290.1:p.Asp332=
XM_017011103.2:c.3966T>C	XP_016866592.1:p.Asp1322=
XM_017011104.1:c.3936T>C	XP_016866593.1:p.Asp1312=
XM_017011105.2:c.3906T>C	XP_016866594.1:p.Asp1302=
XM_017011106.2:c.3777T>C	XP_016866595.1:p.Asp1259=
XM_017011107.2:c.3756T>C	XP_016866596.1:p.Asp1252=
XR_002956289.1:n.4148T>C
NM_001363725.2:c.1605T>C	NP_001350654.1:p.Asp535=
NM_001371656.1:c.3984T>C	NP_001358585.1:p.Asp1328=
NM_001374820.1:c.3984T>C	NP_001361749.1:p.Asp1328=
NM_001374828.1:c.4104T>C MANE Select	NP_001361757.1:p.Asp1368=
NM_017519.3:c.3945T>C	NP_059989.3:p.Asp1315=