Canonical Allele Identifier: CA366241254

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522066G>C (hg19) ; chr6:g.157200932G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200932G>C , CM000668.2:g.157200932G>C	GRCh38
NC_000006.11:g.157522066G>C , CM000668.1:g.157522066G>C	GRCh37
NC_000006.10:g.157563758G>C	NCBI36
NG_032093.1:g.428003G>C
NG_032093.2:g.428003G>C
NG_066624.1:g.429907G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4548G>C	ENSP00000055163.8:p.Gln1516His
ENST00000414678.8:c.4617G>C	ENSP00000412835.3:p.Gln1539His
ENST00000637015.2:c.4836G>C	ENSP00000489729.2:p.Gln1612His
ENST00000346085.10:c.4587G>C	ENSP00000344546.5:p.Gln1529His
ENST00000350026.10:c.4299G>C	ENSP00000055163.7:p.Gln1433His
ENST00000414678.7:c.2865G>C	ENSP00000412835.2:p.Gln955His
ENST00000635849.1:c.2028G>C	ENSP00000490948.1:p.Gln676His
ENST00000635957.1:c.1659G>C	ENSP00000490385.1:p.Gln553His
ENST00000636227.1:n.3170G>C
ENST00000636254.1:n.627G>C
ENST00000636930.2:c.4707G>C MANE Select	ENSP00000490491.2:p.Gln1569His
ENST00000636940.1:n.2704G>C
ENST00000637015.1:c.2075G>C
ENST00000637568.1:c.1989G>C
ENST00000637741.1:n.1373G>C
ENST00000637810.1:c.2049G>C	ENSP00000489636.1:p.Gln683His
ENST00000637904.1:c.2208G>C	ENSP00000490550.1:p.Gln736His
ENST00000647938.1:c.4338G>C	ENSP00000498155.1:p.Gln1446His
ENST00000346085.9:c.4338G>C	ENSP00000344546.4:p.Gln1446His
ENST00000350026.9:c.4299G>C	ENSP00000055163.7:p.Gln1433His
ENST00000414678.6:c.2865G>C	ENSP00000412835.2:p.Gln955His
NM_017519.2:c.4299G>C	NP_059989.2:p.Gln1433His
NM_020732.3:c.4338G>C	NP_065783.3:p.Gln1446His
XM_005267069.3:c.4458G>C	XP_005267126.2:p.Gln1486His
XM_011535984.1:c.3537G>C	XP_011534286.1:p.Gln1179His
XM_011535985.1:c.3357G>C	XP_011534287.1:p.Gln1119His
XM_011535986.1:c.3117G>C	XP_011534288.1:p.Gln1039His
XM_011535987.1:c.2736G>C	XP_011534289.1:p.Gln912His
XM_011535988.1:c.1599G>C	XP_011534290.1:p.Gln533His
NM_001346813.1:c.4458G>C	NP_001333742.1:p.Gln1486His
NM_001363725.1:c.2208G>C	NP_001350654.1:p.Gln736His
XM_011535984.2:c.4668G>C	XP_011534286.2:p.Gln1556His
XM_011535988.3:c.1599G>C	XP_011534290.1:p.Gln533His
XM_017011103.2:c.4569G>C	XP_016866592.1:p.Gln1523His
XM_017011104.1:c.4539G>C	XP_016866593.1:p.Gln1513His
XM_017011105.2:c.4509G>C	XP_016866594.1:p.Gln1503His
XM_017011106.2:c.4380G>C	XP_016866595.1:p.Gln1460His
XM_017011107.2:c.4359G>C	XP_016866596.1:p.Gln1453His
XR_002956289.1:n.4654G>C
NM_001363725.2:c.2208G>C	NP_001350654.1:p.Gln736His
NM_001371656.1:c.4587G>C	NP_001358585.1:p.Gln1529His
NM_001374820.1:c.4587G>C	NP_001361749.1:p.Gln1529His
NM_001374828.1:c.4707G>C MANE Select	NP_001361757.1:p.Gln1569His
NM_017519.3:c.4548G>C	NP_059989.3:p.Gln1516His