Canonical Allele Identifier: CA366234012

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510785G>C (hg19) ; chr6:g.157189651G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189651G>C , CM000668.2:g.157189651G>C	GRCh38
NC_000006.11:g.157510785G>C , CM000668.1:g.157510785G>C	GRCh37
NC_000006.10:g.157552477G>C	NCBI36
NG_032093.1:g.416722G>C
NG_032093.2:g.416722G>C
NG_066624.1:g.418626G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3770G>C	ENSP00000055163.8:p.Gly1257Ala
ENST00000414678.8:c.3839G>C	ENSP00000412835.3:p.Gly1280Ala
ENST00000637015.2:c.4058G>C	ENSP00000489729.2:p.Gly1353Ala
ENST00000346085.10:c.3809G>C	ENSP00000344546.5:p.Gly1270Ala
ENST00000350026.10:c.3521G>C	ENSP00000055163.7:p.Gly1174Ala
ENST00000414678.7:c.2087G>C	ENSP00000412835.2:p.Gly696Ala
ENST00000635849.1:c.1250G>C	ENSP00000490948.1:p.Gly417Ala
ENST00000635957.1:c.884G>C	ENSP00000490385.1:p.Gly295Ala
ENST00000636930.2:c.3929G>C MANE Select	ENSP00000490491.2:p.Gly1310Ala
ENST00000636940.1:n.1926G>C
ENST00000637015.1:c.1297G>C
ENST00000637568.1:c.1211G>C
ENST00000637741.1:n.595G>C
ENST00000637810.1:c.1271G>C	ENSP00000489636.1:p.Gly424Ala
ENST00000637904.1:c.1430G>C	ENSP00000490550.1:p.Gly477Ala
ENST00000647938.1:c.3560G>C	ENSP00000498155.1:p.Gly1187Ala
ENST00000346085.9:c.3560G>C	ENSP00000344546.4:p.Gly1187Ala
ENST00000350026.9:c.3521G>C	ENSP00000055163.7:p.Gly1174Ala
ENST00000414678.6:c.2087G>C	ENSP00000412835.2:p.Gly696Ala
NM_017519.2:c.3521G>C	NP_059989.2:p.Gly1174Ala
NM_020732.3:c.3560G>C	NP_065783.3:p.Gly1187Ala
XM_005267069.3:c.3680G>C	XP_005267126.2:p.Gly1227Ala
XM_011535984.1:c.2759G>C	XP_011534286.1:p.Gly920Ala
XM_011535985.1:c.2579G>C	XP_011534287.1:p.Gly860Ala
XM_011535986.1:c.2339G>C	XP_011534288.1:p.Gly780Ala
XM_011535987.1:c.1958G>C	XP_011534289.1:p.Gly653Ala
XM_011535988.1:c.821G>C	XP_011534290.1:p.Gly274Ala
NM_001346813.1:c.3680G>C	NP_001333742.1:p.Gly1227Ala
NM_001363725.1:c.1430G>C	NP_001350654.1:p.Gly477Ala
XM_011535984.2:c.3890G>C	XP_011534286.2:p.Gly1297Ala
XM_011535988.3:c.821G>C	XP_011534290.1:p.Gly274Ala
XM_017011103.2:c.3791G>C	XP_016866592.1:p.Gly1264Ala
XM_017011104.1:c.3761G>C	XP_016866593.1:p.Gly1254Ala
XM_017011105.2:c.3731G>C	XP_016866594.1:p.Gly1244Ala
XM_017011106.2:c.3602G>C	XP_016866595.1:p.Gly1201Ala
XM_017011107.2:c.3581G>C	XP_016866596.1:p.Gly1194Ala
XR_002956289.1:n.3973G>C
NM_001363725.2:c.1430G>C	NP_001350654.1:p.Gly477Ala
NM_001371656.1:c.3809G>C	NP_001358585.1:p.Gly1270Ala
NM_001374820.1:c.3809G>C	NP_001361749.1:p.Gly1270Ala
NM_001374828.1:c.3929G>C MANE Select	NP_001361757.1:p.Gly1310Ala
NM_017519.3:c.3770G>C	NP_059989.3:p.Gly1257Ala