Canonical Allele Identifier: CA366234019

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510788C>T (hg19) ; chr6:g.157189654C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189654C>T , CM000668.2:g.157189654C>T	GRCh38
NC_000006.11:g.157510788C>T , CM000668.1:g.157510788C>T	GRCh37
NC_000006.10:g.157552480C>T	NCBI36
NG_032093.1:g.416725C>T
NG_032093.2:g.416725C>T
NG_066624.1:g.418629C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3773C>T	ENSP00000055163.8:p.Ser1258Phe
ENST00000414678.8:c.3842C>T	ENSP00000412835.3:p.Ser1281Phe
ENST00000637015.2:c.4061C>T	ENSP00000489729.2:p.Ser1354Phe
ENST00000346085.10:c.3812C>T	ENSP00000344546.5:p.Ser1271Phe
ENST00000350026.10:c.3524C>T	ENSP00000055163.7:p.Ser1175Phe
ENST00000414678.7:c.2090C>T	ENSP00000412835.2:p.Ser697Phe
ENST00000635849.1:c.1253C>T	ENSP00000490948.1:p.Ser418Phe
ENST00000635957.1:c.887C>T	ENSP00000490385.1:p.Ser296Phe
ENST00000636930.2:c.3932C>T MANE Select	ENSP00000490491.2:p.Ser1311Phe
ENST00000636940.1:n.1929C>T
ENST00000637015.1:c.1300C>T
ENST00000637568.1:c.1214C>T
ENST00000637741.1:n.598C>T
ENST00000637810.1:c.1274C>T	ENSP00000489636.1:p.Ser425Phe
ENST00000637904.1:c.1433C>T	ENSP00000490550.1:p.Ser478Phe
ENST00000647938.1:c.3563C>T	ENSP00000498155.1:p.Ser1188Phe
ENST00000346085.9:c.3563C>T	ENSP00000344546.4:p.Ser1188Phe
ENST00000350026.9:c.3524C>T	ENSP00000055163.7:p.Ser1175Phe
ENST00000414678.6:c.2090C>T	ENSP00000412835.2:p.Ser697Phe
NM_017519.2:c.3524C>T	NP_059989.2:p.Ser1175Phe
NM_020732.3:c.3563C>T	NP_065783.3:p.Ser1188Phe
XM_005267069.3:c.3683C>T	XP_005267126.2:p.Ser1228Phe
XM_011535984.1:c.2762C>T	XP_011534286.1:p.Ser921Phe
XM_011535985.1:c.2582C>T	XP_011534287.1:p.Ser861Phe
XM_011535986.1:c.2342C>T	XP_011534288.1:p.Ser781Phe
XM_011535987.1:c.1961C>T	XP_011534289.1:p.Ser654Phe
XM_011535988.1:c.824C>T	XP_011534290.1:p.Ser275Phe
NM_001346813.1:c.3683C>T	NP_001333742.1:p.Ser1228Phe
NM_001363725.1:c.1433C>T	NP_001350654.1:p.Ser478Phe
XM_011535984.2:c.3893C>T	XP_011534286.2:p.Ser1298Phe
XM_011535988.3:c.824C>T	XP_011534290.1:p.Ser275Phe
XM_017011103.2:c.3794C>T	XP_016866592.1:p.Ser1265Phe
XM_017011104.1:c.3764C>T	XP_016866593.1:p.Ser1255Phe
XM_017011105.2:c.3734C>T	XP_016866594.1:p.Ser1245Phe
XM_017011106.2:c.3605C>T	XP_016866595.1:p.Ser1202Phe
XM_017011107.2:c.3584C>T	XP_016866596.1:p.Ser1195Phe
XR_002956289.1:n.3976C>T
NM_001363725.2:c.1433C>T	NP_001350654.1:p.Ser478Phe
NM_001371656.1:c.3812C>T	NP_001358585.1:p.Ser1271Phe
NM_001374820.1:c.3812C>T	NP_001361749.1:p.Ser1271Phe
NM_001374828.1:c.3932C>T MANE Select	NP_001361757.1:p.Ser1311Phe
NM_017519.3:c.3773C>T	NP_059989.3:p.Ser1258Phe