Canonical Allele Identifier: CA366246195

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157527522G>T (hg19) ; chr6:g.157206388G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157206388G>T , CM000668.2:g.157206388G>T	GRCh38
NC_000006.11:g.157527522G>T , CM000668.1:g.157527522G>T	GRCh37
NC_000006.10:g.157569214G>T	NCBI36
NG_032093.1:g.433459G>T
NG_032093.2:g.433459G>T
NG_066624.1:g.435363G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.5457G>T	ENSP00000055163.8:p.Glu1819Asp
ENST00000414678.8:c.5526G>T	ENSP00000412835.3:p.Glu1842Asp
ENST00000637015.2:c.5745G>T	ENSP00000489729.2:p.Glu1915Asp
ENST00000346085.10:c.5496G>T	ENSP00000344546.5:p.Glu1832Asp
ENST00000350026.10:c.5208G>T	ENSP00000055163.7:p.Glu1736Asp
ENST00000414678.7:c.3774G>T	ENSP00000412835.2:p.Glu1258Asp
ENST00000635849.1:c.2937G>T	ENSP00000490948.1:p.Glu979Asp
ENST00000635957.1:c.2568G>T	ENSP00000490385.1:p.Glu856Asp
ENST00000636227.1:n.4079G>T
ENST00000636254.1:n.1536G>T
ENST00000636930.2:c.5616G>T MANE Select	ENSP00000490491.2:p.Glu1872Asp
ENST00000636940.1:n.3613G>T
ENST00000637015.1:c.2984G>T
ENST00000637568.1:c.2898G>T
ENST00000637741.1:n.2282G>T
ENST00000637810.1:c.2958G>T	ENSP00000489636.1:p.Glu986Asp
ENST00000637904.1:c.3117G>T	ENSP00000490550.1:p.Glu1039Asp
ENST00000637933.1:n.2731G>T
ENST00000647938.1:c.5247G>T	ENSP00000498155.1:p.Glu1749Asp
ENST00000346085.9:c.5247G>T	ENSP00000344546.4:p.Glu1749Asp
ENST00000350026.9:c.5208G>T	ENSP00000055163.7:p.Glu1736Asp
ENST00000414678.6:c.3774G>T	ENSP00000412835.2:p.Glu1258Asp
NM_017519.2:c.5208G>T	NP_059989.2:p.Glu1736Asp
NM_020732.3:c.5247G>T	NP_065783.3:p.Glu1749Asp
XM_005267069.3:c.5367G>T	XP_005267126.2:p.Glu1789Asp
XM_011535984.1:c.4446G>T	XP_011534286.1:p.Glu1482Asp
XM_011535985.1:c.4266G>T	XP_011534287.1:p.Glu1422Asp
XM_011535986.1:c.4026G>T	XP_011534288.1:p.Glu1342Asp
XM_011535987.1:c.3645G>T	XP_011534289.1:p.Glu1215Asp
XM_011535988.1:c.2508G>T	XP_011534290.1:p.Glu836Asp
NM_001346813.1:c.5367G>T	NP_001333742.1:p.Glu1789Asp
NM_001363725.1:c.3117G>T	NP_001350654.1:p.Glu1039Asp
XM_011535984.2:c.5577G>T	XP_011534286.2:p.Glu1859Asp
XM_011535988.3:c.2508G>T	XP_011534290.1:p.Glu836Asp
XM_017011103.2:c.5478G>T	XP_016866592.1:p.Glu1826Asp
XM_017011104.1:c.5448G>T	XP_016866593.1:p.Glu1816Asp
XM_017011105.2:c.5418G>T	XP_016866594.1:p.Glu1806Asp
XM_017011106.2:c.5289G>T	XP_016866595.1:p.Glu1763Asp
XM_017011107.2:c.5268G>T	XP_016866596.1:p.Glu1756Asp
XR_002956289.1:n.5563G>T
NM_001363725.2:c.3117G>T	NP_001350654.1:p.Glu1039Asp
NM_001371656.1:c.5496G>T	NP_001358585.1:p.Glu1832Asp
NM_001374820.1:c.5496G>T	NP_001361749.1:p.Glu1832Asp
NM_001374828.1:c.5616G>T MANE Select	NP_001361757.1:p.Glu1872Asp
NM_017519.3:c.5457G>T	NP_059989.3:p.Glu1819Asp