Canonical Allele Identifier: CA366241717

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128374194
• MyVariant Identifiers: chr6:g.157522186G>C (hg19) ; chr6:g.157201052G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201052G>C , CM000668.2:g.157201052G>C	GRCh38
NC_000006.11:g.157522186G>C , CM000668.1:g.157522186G>C	GRCh37
NC_000006.10:g.157563878G>C	NCBI36
NG_032093.1:g.428123G>C
NG_032093.2:g.428123G>C
NG_066624.1:g.430027G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.4668G>C	ENSP00000055163.8:p.Gln1556His
ENST00000414678.8:c.4737G>C	ENSP00000412835.3:p.Gln1579His
ENST00000637015.2:c.4956G>C	ENSP00000489729.2:p.Gln1652His
ENST00000346085.10:c.4707G>C	ENSP00000344546.5:p.Gln1569His
ENST00000350026.10:c.4419G>C	ENSP00000055163.7:p.Gln1473His
ENST00000414678.7:c.2985G>C	ENSP00000412835.2:p.Gln995His
ENST00000635849.1:c.2148G>C	ENSP00000490948.1:p.Gln716His
ENST00000635957.1:c.1779G>C	ENSP00000490385.1:p.Gln593His
ENST00000636227.1:n.3290G>C
ENST00000636254.1:n.747G>C
ENST00000636930.2:c.4827G>C MANE Select	ENSP00000490491.2:p.Gln1609His
ENST00000636940.1:n.2824G>C
ENST00000637015.1:c.2195G>C
ENST00000637568.1:c.2109G>C
ENST00000637741.1:n.1493G>C
ENST00000637810.1:c.2169G>C	ENSP00000489636.1:p.Gln723His
ENST00000637904.1:c.2328G>C	ENSP00000490550.1:p.Gln776His
ENST00000647938.1:c.4458G>C	ENSP00000498155.1:p.Gln1486His
ENST00000346085.9:c.4458G>C	ENSP00000344546.4:p.Gln1486His
ENST00000350026.9:c.4419G>C	ENSP00000055163.7:p.Gln1473His
ENST00000414678.6:c.2985G>C	ENSP00000412835.2:p.Gln995His
NM_017519.2:c.4419G>C	NP_059989.2:p.Gln1473His
NM_020732.3:c.4458G>C	NP_065783.3:p.Gln1486His
XM_005267069.3:c.4578G>C	XP_005267126.2:p.Gln1526His
XM_011535984.1:c.3657G>C	XP_011534286.1:p.Gln1219His
XM_011535985.1:c.3477G>C	XP_011534287.1:p.Gln1159His
XM_011535986.1:c.3237G>C	XP_011534288.1:p.Gln1079His
XM_011535987.1:c.2856G>C	XP_011534289.1:p.Gln952His
XM_011535988.1:c.1719G>C	XP_011534290.1:p.Gln573His
NM_001346813.1:c.4578G>C	NP_001333742.1:p.Gln1526His
NM_001363725.1:c.2328G>C	NP_001350654.1:p.Gln776His
XM_011535984.2:c.4788G>C	XP_011534286.2:p.Gln1596His
XM_011535988.3:c.1719G>C	XP_011534290.1:p.Gln573His
XM_017011103.2:c.4689G>C	XP_016866592.1:p.Gln1563His
XM_017011104.1:c.4659G>C	XP_016866593.1:p.Gln1553His
XM_017011105.2:c.4629G>C	XP_016866594.1:p.Gln1543His
XM_017011106.2:c.4500G>C	XP_016866595.1:p.Gln1500His
XM_017011107.2:c.4479G>C	XP_016866596.1:p.Gln1493His
XR_002956289.1:n.4774G>C
NM_001363725.2:c.2328G>C	NP_001350654.1:p.Gln776His
NM_001371656.1:c.4707G>C	NP_001358585.1:p.Gln1569His
NM_001374820.1:c.4707G>C	NP_001361749.1:p.Gln1569His
NM_001374828.1:c.4827G>C MANE Select	NP_001361757.1:p.Gln1609His
NM_017519.3:c.4668G>C	NP_059989.3:p.Gln1556His