Canonical Allele Identifier: CA452781823

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511226C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190092C>T , CM000668.2:g.157190092C>T	GRCh38
NC_000006.11:g.157511226C>T , CM000668.1:g.157511226C>T	GRCh37
NC_000006.10:g.157552918C>T	NCBI36
NG_032093.1:g.417163C>T
NG_032093.2:g.417163C>T
NG_066624.1:g.419067C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3954C>T	ENSP00000055163.8:p.Phe1318=
ENST00000414678.8:c.4023C>T	ENSP00000412835.3:p.Phe1341=
ENST00000637015.2:c.4242C>T	ENSP00000489729.2:p.Phe1414=
ENST00000346085.10:c.3993C>T	ENSP00000344546.5:p.Phe1331=
ENST00000350026.10:c.3705C>T	ENSP00000055163.7:p.Phe1235=
ENST00000414678.7:c.2271C>T	ENSP00000412835.2:p.Phe757=
ENST00000635849.1:c.1434C>T	ENSP00000490948.1:p.Phe478=
ENST00000635957.1:c.1065C>T	ENSP00000490385.1:p.Phe355=
ENST00000636930.2:c.4113C>T MANE Select	ENSP00000490491.2:p.Phe1371=
ENST00000636940.1:n.2110C>T
ENST00000637015.1:c.1481C>T
ENST00000637568.1:c.1395C>T
ENST00000637741.1:n.779C>T
ENST00000637810.1:c.1455C>T	ENSP00000489636.1:p.Phe485=
ENST00000637904.1:c.1614C>T	ENSP00000490550.1:p.Phe538=
ENST00000647938.1:c.3744C>T	ENSP00000498155.1:p.Phe1248=
ENST00000346085.9:c.3744C>T	ENSP00000344546.4:p.Phe1248=
ENST00000350026.9:c.3705C>T	ENSP00000055163.7:p.Phe1235=
ENST00000414678.6:c.2271C>T	ENSP00000412835.2:p.Phe757=
NM_017519.2:c.3705C>T	NP_059989.2:p.Phe1235=
NM_020732.3:c.3744C>T	NP_065783.3:p.Phe1248=
XM_005267069.3:c.3864C>T	XP_005267126.2:p.Phe1288=
XM_011535984.1:c.2943C>T	XP_011534286.1:p.Phe981=
XM_011535985.1:c.2763C>T	XP_011534287.1:p.Phe921=
XM_011535986.1:c.2523C>T	XP_011534288.1:p.Phe841=
XM_011535987.1:c.2142C>T	XP_011534289.1:p.Phe714=
XM_011535988.1:c.1005C>T	XP_011534290.1:p.Phe335=
NM_001346813.1:c.3864C>T	NP_001333742.1:p.Phe1288=
NM_001363725.1:c.1614C>T	NP_001350654.1:p.Phe538=
XM_011535984.2:c.4074C>T	XP_011534286.2:p.Phe1358=
XM_011535988.3:c.1005C>T	XP_011534290.1:p.Phe335=
XM_017011103.2:c.3975C>T	XP_016866592.1:p.Phe1325=
XM_017011104.1:c.3945C>T	XP_016866593.1:p.Phe1315=
XM_017011105.2:c.3915C>T	XP_016866594.1:p.Phe1305=
XM_017011106.2:c.3786C>T	XP_016866595.1:p.Phe1262=
XM_017011107.2:c.3765C>T	XP_016866596.1:p.Phe1255=
XR_002956289.1:n.4157C>T
NM_001363725.2:c.1614C>T	NP_001350654.1:p.Phe538=
NM_001371656.1:c.3993C>T	NP_001358585.1:p.Phe1331=
NM_001374820.1:c.3993C>T	NP_001361749.1:p.Phe1331=
NM_001374828.1:c.4113C>T MANE Select	NP_001361757.1:p.Phe1371=
NM_017519.3:c.3954C>T	NP_059989.3:p.Phe1318=