Canonical Allele Identifier: CA4067967

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157206944G>A , CM000668.2:g.157206944G>A	GRCh38
NC_000006.11:g.157528078G>A , CM000668.1:g.157528078G>A	GRCh37
NC_000006.10:g.157569770G>A	NCBI36
NG_032093.1:g.434015G>A
NG_032093.2:g.434015G>A
NG_066624.1:g.435919G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001374828.1:c.6172G>A MANE Select	NP_001361757.1:p.Ala2058Thr
ENST00000636930.2:c.6172G>A MANE Select	ENSP00000490491.2:p.Ala2058Thr
NM_001346813.1:c.5923G>A	NP_001333742.1:p.Ala1975Thr
NM_001363725.1:c.3673G>A	NP_001350654.1:p.Ala1225Thr
NM_001363725.2:c.3673G>A	NP_001350654.1:p.Ala1225Thr
NM_001371656.1:c.6052G>A	NP_001358585.1:p.Ala2018Thr
NM_001374820.1:c.6052G>A	NP_001361749.1:p.Ala2018Thr
NM_017519.2:c.5764G>A	NP_059989.2:p.Ala1922Thr
NM_017519.3:c.6013G>A	NP_059989.3:p.Ala2005Thr
NM_020732.3:c.5803G>A	NP_065783.3:p.Ala1935Thr
ENST00000346085.10:c.6052G>A	ENSP00000344546.5:p.Ala2018Thr
ENST00000346085.9:c.5803G>A	ENSP00000344546.4:p.Ala1935Thr
ENST00000350026.10:c.5764G>A	ENSP00000055163.7:p.Ala1922Thr
ENST00000350026.11:c.6013G>A	ENSP00000055163.8:p.Ala2005Thr
ENST00000350026.9:c.5764G>A	ENSP00000055163.7:p.Ala1922Thr
ENST00000414678.6:c.4330G>A	ENSP00000412835.2:p.Ala1444Thr
ENST00000414678.7:c.4330G>A	ENSP00000412835.2:p.Ala1444Thr
ENST00000414678.8:c.6082G>A	ENSP00000412835.3:p.Ala2028Thr
ENST00000635849.1:c.3493G>A	ENSP00000490948.1:p.Ala1165Thr
ENST00000635928.1:c.328G>A	ENSP00000489717.1:p.Ala110Thr
ENST00000635957.1:c.3124G>A	ENSP00000490385.1:p.Ala1042Thr
ENST00000636227.1:n.4635G>A
ENST00000636254.1:n.2092G>A
ENST00000636940.1:n.4169G>A
ENST00000637015.1:c.3540G>A
ENST00000637015.2:c.6301G>A	ENSP00000489729.2:p.Ala2101Thr
ENST00000637568.1:c.3454G>A
ENST00000637741.1:n.2838G>A
ENST00000637810.1:c.3514G>A	ENSP00000489636.1:p.Ala1172Thr
ENST00000637904.1:c.3673G>A	ENSP00000490550.1:p.Ala1225Thr
ENST00000637933.1:n.3287G>A
ENST00000647938.1:c.5803G>A	ENSP00000498155.1:p.Ala1935Thr
XM_005267069.3:c.5923G>A	XP_005267126.2:p.Ala1975Thr
XM_011535984.1:c.5002G>A	XP_011534286.1:p.Ala1668Thr
XM_011535984.2:c.6133G>A	XP_011534286.2:p.Ala2045Thr
XM_011535985.1:c.4822G>A	XP_011534287.1:p.Ala1608Thr
XM_011535986.1:c.4582G>A	XP_011534288.1:p.Ala1528Thr
XM_011535987.1:c.4201G>A	XP_011534289.1:p.Ala1401Thr
XM_011535988.1:c.3064G>A	XP_011534290.1:p.Ala1022Thr
XM_011535988.3:c.3064G>A	XP_011534290.1:p.Ala1022Thr
XM_017011103.2:c.6034G>A	XP_016866592.1:p.Ala2012Thr
XM_017011104.1:c.6004G>A	XP_016866593.1:p.Ala2002Thr
XM_017011105.2:c.5974G>A	XP_016866594.1:p.Ala1992Thr
XM_017011106.2:c.5845G>A	XP_016866595.1:p.Ala1949Thr
XM_017011107.2:c.5824G>A	XP_016866596.1:p.Ala1942Thr
XR_002956289.1:n.6119G>A