Canonical Allele Identifier: CA366235064

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511217T>G (hg19) ; chr6:g.157190083T>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3945T>G	ENSP00000055163.8:p.Asp1315Glu
ENST00000414678.8:c.4014T>G	ENSP00000412835.3:p.Asp1338Glu
ENST00000637015.2:c.4233T>G	ENSP00000489729.2:p.Asp1411Glu
ENST00000346085.10:c.3984T>G	ENSP00000344546.5:p.Asp1328Glu
ENST00000350026.10:c.3696T>G	ENSP00000055163.7:p.Asp1232Glu
ENST00000414678.7:c.2262T>G	ENSP00000412835.2:p.Asp754Glu
ENST00000635849.1:c.1425T>G	ENSP00000490948.1:p.Asp475Glu
ENST00000635957.1:c.1056T>G	ENSP00000490385.1:p.Asp352Glu
ENST00000636930.2:c.4104T>G MANE Select	ENSP00000490491.2:p.Asp1368Glu
ENST00000636940.1:n.2101T>G
ENST00000637015.1:c.1472T>G
ENST00000637568.1:c.1386T>G
ENST00000637741.1:n.770T>G
ENST00000637810.1:c.1446T>G	ENSP00000489636.1:p.Asp482Glu
ENST00000637904.1:c.1605T>G	ENSP00000490550.1:p.Asp535Glu
ENST00000647938.1:c.3735T>G	ENSP00000498155.1:p.Asp1245Glu
ENST00000346085.9:c.3735T>G	ENSP00000344546.4:p.Asp1245Glu
ENST00000350026.9:c.3696T>G	ENSP00000055163.7:p.Asp1232Glu
ENST00000414678.6:c.2262T>G	ENSP00000412835.2:p.Asp754Glu
NM_017519.2:c.3696T>G	NP_059989.2:p.Asp1232Glu
NM_020732.3:c.3735T>G	NP_065783.3:p.Asp1245Glu
XM_005267069.3:c.3855T>G	XP_005267126.2:p.Asp1285Glu
XM_011535984.1:c.2934T>G	XP_011534286.1:p.Asp978Glu
XM_011535985.1:c.2754T>G	XP_011534287.1:p.Asp918Glu
XM_011535986.1:c.2514T>G	XP_011534288.1:p.Asp838Glu
XM_011535987.1:c.2133T>G	XP_011534289.1:p.Asp711Glu
XM_011535988.1:c.996T>G	XP_011534290.1:p.Asp332Glu
NM_001346813.1:c.3855T>G	NP_001333742.1:p.Asp1285Glu
NM_001363725.1:c.1605T>G	NP_001350654.1:p.Asp535Glu
XM_011535984.2:c.4065T>G	XP_011534286.2:p.Asp1355Glu
XM_011535988.3:c.996T>G	XP_011534290.1:p.Asp332Glu
XM_017011103.2:c.3966T>G	XP_016866592.1:p.Asp1322Glu
XM_017011104.1:c.3936T>G	XP_016866593.1:p.Asp1312Glu
XM_017011105.2:c.3906T>G	XP_016866594.1:p.Asp1302Glu
XM_017011106.2:c.3777T>G	XP_016866595.1:p.Asp1259Glu
XM_017011107.2:c.3756T>G	XP_016866596.1:p.Asp1252Glu
XR_002956289.1:n.4148T>G
NM_001363725.2:c.1605T>G	NP_001350654.1:p.Asp535Glu
NM_001371656.1:c.3984T>G	NP_001358585.1:p.Asp1328Glu
NM_001374820.1:c.3984T>G	NP_001361749.1:p.Asp1328Glu
NM_001374828.1:c.4104T>G MANE Select	NP_001361757.1:p.Asp1368Glu
NM_017519.3:c.3945T>G	NP_059989.3:p.Asp1315Glu