Canonical Allele Identifier: CA366234156

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128338888
• MyVariant Identifiers: chr6:g.157510852C>G (hg19) ; chr6:g.157189718C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189718C>G , CM000668.2:g.157189718C>G	GRCh38
NC_000006.11:g.157510852C>G , CM000668.1:g.157510852C>G	GRCh37
NC_000006.10:g.157552544C>G	NCBI36
NG_032093.1:g.416789C>G
NG_032093.2:g.416789C>G
NG_066624.1:g.418693C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3837C>G	ENSP00000055163.8:p.Asp1279Glu
ENST00000414678.8:c.3906C>G	ENSP00000412835.3:p.Asp1302Glu
ENST00000637015.2:c.4125C>G	ENSP00000489729.2:p.Asp1375Glu
ENST00000346085.10:c.3876C>G	ENSP00000344546.5:p.Asp1292Glu
ENST00000350026.10:c.3588C>G	ENSP00000055163.7:p.Asp1196Glu
ENST00000414678.7:c.2154C>G	ENSP00000412835.2:p.Asp718Glu
ENST00000635849.1:c.1317C>G	ENSP00000490948.1:p.Asp439Glu
ENST00000635957.1:c.951C>G	ENSP00000490385.1:p.Asp317Glu
ENST00000636930.2:c.3996C>G MANE Select	ENSP00000490491.2:p.Asp1332Glu
ENST00000636940.1:n.1993C>G
ENST00000637015.1:c.1364C>G
ENST00000637568.1:c.1278C>G
ENST00000637741.1:n.662C>G
ENST00000637810.1:c.1338C>G	ENSP00000489636.1:p.Asp446Glu
ENST00000637904.1:c.1497C>G	ENSP00000490550.1:p.Asp499Glu
ENST00000647938.1:c.3627C>G	ENSP00000498155.1:p.Asp1209Glu
ENST00000346085.9:c.3627C>G	ENSP00000344546.4:p.Asp1209Glu
ENST00000350026.9:c.3588C>G	ENSP00000055163.7:p.Asp1196Glu
ENST00000414678.6:c.2154C>G	ENSP00000412835.2:p.Asp718Glu
NM_017519.2:c.3588C>G	NP_059989.2:p.Asp1196Glu
NM_020732.3:c.3627C>G	NP_065783.3:p.Asp1209Glu
XM_005267069.3:c.3747C>G	XP_005267126.2:p.Asp1249Glu
XM_011535984.1:c.2826C>G	XP_011534286.1:p.Asp942Glu
XM_011535985.1:c.2646C>G	XP_011534287.1:p.Asp882Glu
XM_011535986.1:c.2406C>G	XP_011534288.1:p.Asp802Glu
XM_011535987.1:c.2025C>G	XP_011534289.1:p.Asp675Glu
XM_011535988.1:c.888C>G	XP_011534290.1:p.Asp296Glu
NM_001346813.1:c.3747C>G	NP_001333742.1:p.Asp1249Glu
NM_001363725.1:c.1497C>G	NP_001350654.1:p.Asp499Glu
XM_011535984.2:c.3957C>G	XP_011534286.2:p.Asp1319Glu
XM_011535988.3:c.888C>G	XP_011534290.1:p.Asp296Glu
XM_017011103.2:c.3858C>G	XP_016866592.1:p.Asp1286Glu
XM_017011104.1:c.3828C>G	XP_016866593.1:p.Asp1276Glu
XM_017011105.2:c.3798C>G	XP_016866594.1:p.Asp1266Glu
XM_017011106.2:c.3669C>G	XP_016866595.1:p.Asp1223Glu
XM_017011107.2:c.3648C>G	XP_016866596.1:p.Asp1216Glu
XR_002956289.1:n.4040C>G
NM_001363725.2:c.1497C>G	NP_001350654.1:p.Asp499Glu
NM_001371656.1:c.3876C>G	NP_001358585.1:p.Asp1292Glu
NM_001374820.1:c.3876C>G	NP_001361749.1:p.Asp1292Glu
NM_001374828.1:c.3996C>G MANE Select	NP_001361757.1:p.Asp1332Glu
NM_017519.3:c.3837C>G	NP_059989.3:p.Asp1279Glu