Canonical Allele Identifier: CA366234144

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510847G>C (hg19) ; chr6:g.157189713G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189713G>C , CM000668.2:g.157189713G>C	GRCh38
NC_000006.11:g.157510847G>C , CM000668.1:g.157510847G>C	GRCh37
NC_000006.10:g.157552539G>C	NCBI36
NG_032093.1:g.416784G>C
NG_032093.2:g.416784G>C
NG_066624.1:g.418688G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3832G>C	ENSP00000055163.8:p.Gly1278Arg
ENST00000414678.8:c.3901G>C	ENSP00000412835.3:p.Gly1301Arg
ENST00000637015.2:c.4120G>C	ENSP00000489729.2:p.Gly1374Arg
ENST00000346085.10:c.3871G>C	ENSP00000344546.5:p.Gly1291Arg
ENST00000350026.10:c.3583G>C	ENSP00000055163.7:p.Gly1195Arg
ENST00000414678.7:c.2149G>C	ENSP00000412835.2:p.Gly717Arg
ENST00000635849.1:c.1312G>C	ENSP00000490948.1:p.Gly438Arg
ENST00000635957.1:c.946G>C	ENSP00000490385.1:p.Gly316Arg
ENST00000636930.2:c.3991G>C MANE Select	ENSP00000490491.2:p.Gly1331Arg
ENST00000636940.1:n.1988G>C
ENST00000637015.1:c.1359G>C
ENST00000637568.1:c.1273G>C
ENST00000637741.1:n.657G>C
ENST00000637810.1:c.1333G>C	ENSP00000489636.1:p.Gly445Arg
ENST00000637904.1:c.1492G>C	ENSP00000490550.1:p.Gly498Arg
ENST00000647938.1:c.3622G>C	ENSP00000498155.1:p.Gly1208Arg
ENST00000346085.9:c.3622G>C	ENSP00000344546.4:p.Gly1208Arg
ENST00000350026.9:c.3583G>C	ENSP00000055163.7:p.Gly1195Arg
ENST00000414678.6:c.2149G>C	ENSP00000412835.2:p.Gly717Arg
NM_017519.2:c.3583G>C	NP_059989.2:p.Gly1195Arg
NM_020732.3:c.3622G>C	NP_065783.3:p.Gly1208Arg
XM_005267069.3:c.3742G>C	XP_005267126.2:p.Gly1248Arg
XM_011535984.1:c.2821G>C	XP_011534286.1:p.Gly941Arg
XM_011535985.1:c.2641G>C	XP_011534287.1:p.Gly881Arg
XM_011535986.1:c.2401G>C	XP_011534288.1:p.Gly801Arg
XM_011535987.1:c.2020G>C	XP_011534289.1:p.Gly674Arg
XM_011535988.1:c.883G>C	XP_011534290.1:p.Gly295Arg
NM_001346813.1:c.3742G>C	NP_001333742.1:p.Gly1248Arg
NM_001363725.1:c.1492G>C	NP_001350654.1:p.Gly498Arg
XM_011535984.2:c.3952G>C	XP_011534286.2:p.Gly1318Arg
XM_011535988.3:c.883G>C	XP_011534290.1:p.Gly295Arg
XM_017011103.2:c.3853G>C	XP_016866592.1:p.Gly1285Arg
XM_017011104.1:c.3823G>C	XP_016866593.1:p.Gly1275Arg
XM_017011105.2:c.3793G>C	XP_016866594.1:p.Gly1265Arg
XM_017011106.2:c.3664G>C	XP_016866595.1:p.Gly1222Arg
XM_017011107.2:c.3643G>C	XP_016866596.1:p.Gly1215Arg
XR_002956289.1:n.4035G>C
NM_001363725.2:c.1492G>C	NP_001350654.1:p.Gly498Arg
NM_001371656.1:c.3871G>C	NP_001358585.1:p.Gly1291Arg
NM_001374820.1:c.3871G>C	NP_001361749.1:p.Gly1291Arg
NM_001374828.1:c.3991G>C MANE Select	NP_001361757.1:p.Gly1331Arg
NM_017519.3:c.3832G>C	NP_059989.3:p.Gly1278Arg