Canonical Allele Identifier: CA366242811

Gene: ARID1B

Linked Data

• dbSNP Id: rs944809709
• MyVariant Identifiers: chr6:g.157522509G>C (hg19) ; chr6:g.157201375G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201375G>C , CM000668.2:g.157201375G>C	GRCh38
NC_000006.11:g.157522509G>C , CM000668.1:g.157522509G>C	GRCh37
NC_000006.10:g.157564201G>C	NCBI36
NG_032093.1:g.428446G>C
NG_032093.2:g.428446G>C
NG_066624.1:g.430350G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4991G>C	ENSP00000055163.8:p.Gly1664Ala
ENST00000414678.8:c.5060G>C	ENSP00000412835.3:p.Gly1687Ala
ENST00000637015.2:c.5279G>C	ENSP00000489729.2:p.Gly1760Ala
ENST00000346085.10:c.5030G>C	ENSP00000344546.5:p.Gly1677Ala
ENST00000350026.10:c.4742G>C	ENSP00000055163.7:p.Gly1581Ala
ENST00000414678.7:c.3308G>C	ENSP00000412835.2:p.Gly1103Ala
ENST00000635849.1:c.2471G>C	ENSP00000490948.1:p.Gly824Ala
ENST00000635957.1:c.2102G>C	ENSP00000490385.1:p.Gly701Ala
ENST00000636227.1:n.3613G>C
ENST00000636254.1:n.1070G>C
ENST00000636930.2:c.5150G>C MANE Select	ENSP00000490491.2:p.Gly1717Ala
ENST00000636940.1:n.3147G>C
ENST00000637015.1:c.2518G>C
ENST00000637568.1:c.2432G>C
ENST00000637741.1:n.1816G>C
ENST00000637810.1:c.2492G>C	ENSP00000489636.1:p.Gly831Ala
ENST00000637904.1:c.2651G>C	ENSP00000490550.1:p.Gly884Ala
ENST00000647938.1:c.4781G>C	ENSP00000498155.1:p.Gly1594Ala
ENST00000346085.9:c.4781G>C	ENSP00000344546.4:p.Gly1594Ala
ENST00000350026.9:c.4742G>C	ENSP00000055163.7:p.Gly1581Ala
ENST00000414678.6:c.3308G>C	ENSP00000412835.2:p.Gly1103Ala
NM_017519.2:c.4742G>C	NP_059989.2:p.Gly1581Ala
NM_020732.3:c.4781G>C	NP_065783.3:p.Gly1594Ala
XM_005267069.3:c.4901G>C	XP_005267126.2:p.Gly1634Ala
XM_011535984.1:c.3980G>C	XP_011534286.1:p.Gly1327Ala
XM_011535985.1:c.3800G>C	XP_011534287.1:p.Gly1267Ala
XM_011535986.1:c.3560G>C	XP_011534288.1:p.Gly1187Ala
XM_011535987.1:c.3179G>C	XP_011534289.1:p.Gly1060Ala
XM_011535988.1:c.2042G>C	XP_011534290.1:p.Gly681Ala
NM_001346813.1:c.4901G>C	NP_001333742.1:p.Gly1634Ala
NM_001363725.1:c.2651G>C	NP_001350654.1:p.Gly884Ala
XM_011535984.2:c.5111G>C	XP_011534286.2:p.Gly1704Ala
XM_011535988.3:c.2042G>C	XP_011534290.1:p.Gly681Ala
XM_017011103.2:c.5012G>C	XP_016866592.1:p.Gly1671Ala
XM_017011104.1:c.4982G>C	XP_016866593.1:p.Gly1661Ala
XM_017011105.2:c.4952G>C	XP_016866594.1:p.Gly1651Ala
XM_017011106.2:c.4823G>C	XP_016866595.1:p.Gly1608Ala
XM_017011107.2:c.4802G>C	XP_016866596.1:p.Gly1601Ala
XR_002956289.1:n.5097G>C
NM_001363725.2:c.2651G>C	NP_001350654.1:p.Gly884Ala
NM_001371656.1:c.5030G>C	NP_001358585.1:p.Gly1677Ala
NM_001374820.1:c.5030G>C	NP_001361749.1:p.Gly1677Ala
NM_001374828.1:c.5150G>C MANE Select	NP_001361757.1:p.Gly1717Ala
NM_017519.3:c.4991G>C	NP_059989.3:p.Gly1664Ala