Canonical Allele Identifier: CA366241249

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522064C>A (hg19) ; chr6:g.157200930C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200930C>A , CM000668.2:g.157200930C>A	GRCh38
NC_000006.11:g.157522064C>A , CM000668.1:g.157522064C>A	GRCh37
NC_000006.10:g.157563756C>A	NCBI36
NG_032093.1:g.428001C>A
NG_032093.2:g.428001C>A
NG_066624.1:g.429905C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4546C>A	ENSP00000055163.8:p.Gln1516Lys
ENST00000414678.8:c.4615C>A	ENSP00000412835.3:p.Gln1539Lys
ENST00000637015.2:c.4834C>A	ENSP00000489729.2:p.Gln1612Lys
ENST00000346085.10:c.4585C>A	ENSP00000344546.5:p.Gln1529Lys
ENST00000350026.10:c.4297C>A	ENSP00000055163.7:p.Gln1433Lys
ENST00000414678.7:c.2863C>A	ENSP00000412835.2:p.Gln955Lys
ENST00000635849.1:c.2026C>A	ENSP00000490948.1:p.Gln676Lys
ENST00000635957.1:c.1657C>A	ENSP00000490385.1:p.Gln553Lys
ENST00000636227.1:n.3168C>A
ENST00000636254.1:n.625C>A
ENST00000636930.2:c.4705C>A MANE Select	ENSP00000490491.2:p.Gln1569Lys
ENST00000636940.1:n.2702C>A
ENST00000637015.1:c.2073C>A
ENST00000637568.1:c.1987C>A
ENST00000637741.1:n.1371C>A
ENST00000637810.1:c.2047C>A	ENSP00000489636.1:p.Gln683Lys
ENST00000637904.1:c.2206C>A	ENSP00000490550.1:p.Gln736Lys
ENST00000647938.1:c.4336C>A	ENSP00000498155.1:p.Gln1446Lys
ENST00000346085.9:c.4336C>A	ENSP00000344546.4:p.Gln1446Lys
ENST00000350026.9:c.4297C>A	ENSP00000055163.7:p.Gln1433Lys
ENST00000414678.6:c.2863C>A	ENSP00000412835.2:p.Gln955Lys
NM_017519.2:c.4297C>A	NP_059989.2:p.Gln1433Lys
NM_020732.3:c.4336C>A	NP_065783.3:p.Gln1446Lys
XM_005267069.3:c.4456C>A	XP_005267126.2:p.Gln1486Lys
XM_011535984.1:c.3535C>A	XP_011534286.1:p.Gln1179Lys
XM_011535985.1:c.3355C>A	XP_011534287.1:p.Gln1119Lys
XM_011535986.1:c.3115C>A	XP_011534288.1:p.Gln1039Lys
XM_011535987.1:c.2734C>A	XP_011534289.1:p.Gln912Lys
XM_011535988.1:c.1597C>A	XP_011534290.1:p.Gln533Lys
NM_001346813.1:c.4456C>A	NP_001333742.1:p.Gln1486Lys
NM_001363725.1:c.2206C>A	NP_001350654.1:p.Gln736Lys
XM_011535984.2:c.4666C>A	XP_011534286.2:p.Gln1556Lys
XM_011535988.3:c.1597C>A	XP_011534290.1:p.Gln533Lys
XM_017011103.2:c.4567C>A	XP_016866592.1:p.Gln1523Lys
XM_017011104.1:c.4537C>A	XP_016866593.1:p.Gln1513Lys
XM_017011105.2:c.4507C>A	XP_016866594.1:p.Gln1503Lys
XM_017011106.2:c.4378C>A	XP_016866595.1:p.Gln1460Lys
XM_017011107.2:c.4357C>A	XP_016866596.1:p.Gln1453Lys
XR_002956289.1:n.4652C>A
NM_001363725.2:c.2206C>A	NP_001350654.1:p.Gln736Lys
NM_001371656.1:c.4585C>A	NP_001358585.1:p.Gln1529Lys
NM_001374820.1:c.4585C>A	NP_001361749.1:p.Gln1529Lys
NM_001374828.1:c.4705C>A MANE Select	NP_001361757.1:p.Gln1569Lys
NM_017519.3:c.4546C>A	NP_059989.3:p.Gln1516Lys