Canonical Allele Identifier: CA366384444

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128046883
• MyVariant Identifiers: chr6:g.157150507G>C (hg19) ; chr6:g.156829373G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.156829373G>C , CM000668.2:g.156829373G>C	GRCh38
NC_000006.11:g.157150507G>C , CM000668.1:g.157150507G>C	GRCh37
NC_000006.10:g.157192199G>C	NCBI36
NG_032093.1:g.56444G>C
NG_032093.2:g.56444G>C
NG_066624.1:g.58348G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.1938G>C	ENSP00000055163.8:p.Gln646His
ENST00000414678.8:c.1938G>C	ENSP00000412835.3:p.Gln646His
ENST00000637015.2:c.1938G>C	ENSP00000489729.2:p.Gln646His
ENST00000346085.10:c.1938G>C	ENSP00000344546.5:p.Gln646His
ENST00000350026.10:c.1689G>C	ENSP00000055163.7:p.Gln563His
ENST00000414678.7:c.186G>C	ENSP00000412835.2:p.Gln62His
ENST00000494260.2:c.219G>C	ENSP00000490094.1:p.Gln73His
ENST00000636205.1:n.1G>C
ENST00000636607.1:c.201G>C	ENSP00000490050.1:p.Gln67His
ENST00000636748.1:c.219G>C	ENSP00000489917.1:p.Gln73His
ENST00000636930.2:c.1938G>C MANE Select	ENSP00000490491.2:p.Gln646His
ENST00000637910.1:n.219G>C
ENST00000638000.1:c.155G>C
ENST00000647938.1:c.1689G>C	ENSP00000498155.1:p.Gln563His
ENST00000674190.1:n.645G>C
ENST00000674298.1:c.1678G>C
ENST00000346085.9:c.1689G>C	ENSP00000344546.4:p.Gln563His
ENST00000350026.9:c.1689G>C	ENSP00000055163.7:p.Gln563His
ENST00000414678.6:c.186G>C	ENSP00000412835.2:p.Gln62His
ENST00000494260.1:n.147G>C
NM_017519.2:c.1689G>C	NP_059989.2:p.Gln563His
NM_020732.3:c.1689G>C	NP_065783.3:p.Gln563His
XM_005267069.3:c.1689G>C	XP_005267126.2:p.Gln563His
XM_011535984.1:c.558G>C	XP_011534286.1:p.Gln186His
XM_011535985.1:c.558G>C	XP_011534287.1:p.Gln186His
XM_011535986.1:c.138G>C	XP_011534288.1:p.Gln46His
NM_001346813.1:c.1689G>C	NP_001333742.1:p.Gln563His
XM_011535984.2:c.1689G>C	XP_011534286.2:p.Gln563His
XM_017011103.2:c.1689G>C	XP_016866592.1:p.Gln563His
XM_017011104.1:c.1689G>C	XP_016866593.1:p.Gln563His
XM_017011105.2:c.1689G>C	XP_016866594.1:p.Gln563His
XM_017011106.2:c.1689G>C	XP_016866595.1:p.Gln563His
XM_017011107.2:c.1689G>C	XP_016866596.1:p.Gln563His
XR_002956289.1:n.1772G>C
NM_001371656.1:c.1938G>C	NP_001358585.1:p.Gln646His
NM_001374820.1:c.1938G>C	NP_001361749.1:p.Gln646His
NM_001374828.1:c.1938G>C MANE Select	NP_001361757.1:p.Gln646His
NM_017519.3:c.1938G>C	NP_059989.3:p.Gln646His