Canonical Allele Identifier: CA452781596

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511202C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190068C>T , CM000668.2:g.157190068C>T	GRCh38
NC_000006.11:g.157511202C>T , CM000668.1:g.157511202C>T	GRCh37
NC_000006.10:g.157552894C>T	NCBI36
NG_032093.1:g.417139C>T
NG_032093.2:g.417139C>T
NG_066624.1:g.419043C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3930C>T	ENSP00000055163.8:p.Phe1310=
ENST00000414678.8:c.3999C>T	ENSP00000412835.3:p.Phe1333=
ENST00000637015.2:c.4218C>T	ENSP00000489729.2:p.Phe1406=
ENST00000346085.10:c.3969C>T	ENSP00000344546.5:p.Phe1323=
ENST00000350026.10:c.3681C>T	ENSP00000055163.7:p.Phe1227=
ENST00000414678.7:c.2247C>T	ENSP00000412835.2:p.Phe749=
ENST00000635849.1:c.1410C>T	ENSP00000490948.1:p.Phe470=
ENST00000635957.1:c.1041C>T	ENSP00000490385.1:p.Phe347=
ENST00000636930.2:c.4089C>T MANE Select	ENSP00000490491.2:p.Phe1363=
ENST00000636940.1:n.2086C>T
ENST00000637015.1:c.1457C>T
ENST00000637568.1:c.1371C>T
ENST00000637741.1:n.755C>T
ENST00000637810.1:c.1431C>T	ENSP00000489636.1:p.Phe477=
ENST00000637904.1:c.1590C>T	ENSP00000490550.1:p.Phe530=
ENST00000647938.1:c.3720C>T	ENSP00000498155.1:p.Phe1240=
ENST00000346085.9:c.3720C>T	ENSP00000344546.4:p.Phe1240=
ENST00000350026.9:c.3681C>T	ENSP00000055163.7:p.Phe1227=
ENST00000414678.6:c.2247C>T	ENSP00000412835.2:p.Phe749=
NM_017519.2:c.3681C>T	NP_059989.2:p.Phe1227=
NM_020732.3:c.3720C>T	NP_065783.3:p.Phe1240=
XM_005267069.3:c.3840C>T	XP_005267126.2:p.Phe1280=
XM_011535984.1:c.2919C>T	XP_011534286.1:p.Phe973=
XM_011535985.1:c.2739C>T	XP_011534287.1:p.Phe913=
XM_011535986.1:c.2499C>T	XP_011534288.1:p.Phe833=
XM_011535987.1:c.2118C>T	XP_011534289.1:p.Phe706=
XM_011535988.1:c.981C>T	XP_011534290.1:p.Phe327=
NM_001346813.1:c.3840C>T	NP_001333742.1:p.Phe1280=
NM_001363725.1:c.1590C>T	NP_001350654.1:p.Phe530=
XM_011535984.2:c.4050C>T	XP_011534286.2:p.Phe1350=
XM_011535988.3:c.981C>T	XP_011534290.1:p.Phe327=
XM_017011103.2:c.3951C>T	XP_016866592.1:p.Phe1317=
XM_017011104.1:c.3921C>T	XP_016866593.1:p.Phe1307=
XM_017011105.2:c.3891C>T	XP_016866594.1:p.Phe1297=
XM_017011106.2:c.3762C>T	XP_016866595.1:p.Phe1254=
XM_017011107.2:c.3741C>T	XP_016866596.1:p.Phe1247=
XR_002956289.1:n.4133C>T
NM_001363725.2:c.1590C>T	NP_001350654.1:p.Phe530=
NM_001371656.1:c.3969C>T	NP_001358585.1:p.Phe1323=
NM_001374820.1:c.3969C>T	NP_001361749.1:p.Phe1323=
NM_001374828.1:c.4089C>T MANE Select	NP_001361757.1:p.Phe1363=
NM_017519.3:c.3930C>T	NP_059989.3:p.Phe1310=