Canonical Allele Identifier: CA207495

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157207735G>A , CM000668.2:g.157207735G>A	GRCh38
NC_000006.11:g.157528869G>A , CM000668.1:g.157528869G>A	GRCh37
NC_000006.10:g.157570561G>A	NCBI36
NG_032093.1:g.434806G>A
NG_032093.2:g.434806G>A
NG_066624.1:g.436710G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001374828.1:c.6963G>A MANE Select	NP_001361757.1:p.Ala2321=
ENST00000636930.2:c.6963G>A MANE Select	ENSP00000490491.2:p.Ala2321=
NM_001346813.1:c.6714G>A	NP_001333742.1:p.Ala2238=
NM_001363725.1:c.4464G>A	NP_001350654.1:p.Ala1488=
NM_001363725.2:c.4464G>A	NP_001350654.1:p.Ala1488=
NM_001371656.1:c.6843G>A	NP_001358585.1:p.Ala2281=
NM_001374820.1:c.6843G>A	NP_001361749.1:p.Ala2281=
NM_017519.2:c.6555G>A	NP_059989.2:p.Ala2185=
NM_017519.3:c.6804G>A	NP_059989.3:p.Ala2268=
NM_020732.3:c.6594G>A	NP_065783.3:p.Ala2198=
ENST00000346085.10:c.6843G>A	ENSP00000344546.5:p.Ala2281=
ENST00000346085.9:c.6594G>A	ENSP00000344546.4:p.Ala2198=
ENST00000350026.10:c.6555G>A	ENSP00000055163.7:p.Ala2185=
ENST00000350026.11:c.6804G>A	ENSP00000055163.8:p.Ala2268=
ENST00000350026.9:c.6555G>A	ENSP00000055163.7:p.Ala2185=
ENST00000414678.6:c.5121G>A	ENSP00000412835.2:p.Ala1707=
ENST00000414678.7:c.5121G>A	ENSP00000412835.2:p.Ala1707=
ENST00000414678.8:c.6873G>A	ENSP00000412835.3:p.Ala2291=
ENST00000635849.1:c.4284G>A	ENSP00000490948.1:p.Ala1428=
ENST00000635928.1:c.875+244G>A	ENSP00000489717.1:n.875+244G>A
ENST00000635957.1:c.3915G>A	ENSP00000490385.1:p.Ala1305=
ENST00000636227.1:n.5426G>A
ENST00000636254.1:n.2883G>A
ENST00000636940.1:n.4960G>A
ENST00000637015.1:c.4331G>A
ENST00000637015.2:c.7092G>A	ENSP00000489729.2:p.Ala2364=
ENST00000637568.1:c.4245G>A
ENST00000637741.1:n.3629G>A
ENST00000637810.1:c.4305G>A	ENSP00000489636.1:p.Ala1435=
ENST00000637904.1:c.4464G>A	ENSP00000490550.1:p.Ala1488=
ENST00000637933.1:n.4078G>A
ENST00000647938.1:c.6594G>A	ENSP00000498155.1:p.Ala2198=
XM_005267069.3:c.6714G>A	XP_005267126.2:p.Ala2238=
XM_011535984.1:c.5793G>A	XP_011534286.1:p.Ala1931=
XM_011535984.2:c.6924G>A	XP_011534286.2:p.Ala2308=
XM_011535985.1:c.5613G>A	XP_011534287.1:p.Ala1871=
XM_011535986.1:c.5373G>A	XP_011534288.1:p.Ala1791=
XM_011535987.1:c.4992G>A	XP_011534289.1:p.Ala1664=
XM_011535988.1:c.3855G>A	XP_011534290.1:p.Ala1285=
XM_011535988.3:c.3855G>A	XP_011534290.1:p.Ala1285=
XM_017011103.2:c.6825G>A	XP_016866592.1:p.Ala2275=
XM_017011104.1:c.6795G>A	XP_016866593.1:p.Ala2265=
XM_017011105.2:c.6765G>A	XP_016866594.1:p.Ala2255=
XM_017011106.2:c.6636G>A	XP_016866595.1:p.Ala2212=
XM_017011107.2:c.6615G>A	XP_016866596.1:p.Ala2205=
XR_002956289.1:n.6910G>A