Canonical Allele Identifier: CA366389210

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157470037A>T (hg19) ; chr6:g.157148903A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148903A>T , CM000668.2:g.157148903A>T	GRCh38
NC_000006.11:g.157470037A>T , CM000668.1:g.157470037A>T	GRCh37
NC_000006.10:g.157511729A>T	NCBI36
NG_032093.1:g.375974A>T
NG_032093.2:g.375974A>T
NG_066624.1:g.377878A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3041A>T	ENSP00000055163.8:p.Glu1014Val
ENST00000414678.8:c.2951A>T	ENSP00000412835.3:p.Glu984Val
ENST00000637015.2:c.3041A>T	ENSP00000489729.2:p.Glu1014Val
ENST00000319584.11:c.1055A>T	ENSP00000313006.7:p.Glu352Val
ENST00000346085.10:c.3080A>T	ENSP00000344546.5:p.Glu1027Val
ENST00000350026.10:c.2792A>T	ENSP00000055163.7:p.Glu931Val
ENST00000414678.7:c.1199A>T	ENSP00000412835.2:p.Glu400Val
ENST00000452544.2:n.942A>T
ENST00000635849.1:c.362A>T	ENSP00000490948.1:p.Glu121Val
ENST00000636426.1:n.175A>T
ENST00000636930.2:c.3041A>T MANE Select	ENSP00000490491.2:p.Glu1014Val
ENST00000637015.1:c.280A>T
ENST00000637568.1:c.84A>T
ENST00000637810.1:c.542A>T	ENSP00000489636.1:p.Glu181Val
ENST00000637904.1:c.542A>T	ENSP00000490550.1:p.Glu181Val
ENST00000647938.1:c.2831A>T	ENSP00000498155.1:p.Glu944Val
ENST00000674190.1:n.1790A>T
ENST00000319584.10:c.1058A>T	ENSP00000313006.6:p.Glu353Val
ENST00000346085.9:c.2831A>T	ENSP00000344546.4:p.Glu944Val
ENST00000350026.9:c.2792A>T	ENSP00000055163.7:p.Glu931Val
ENST00000414678.6:c.1199A>T	ENSP00000412835.2:p.Glu400Val
ENST00000452544.1:n.888A>T
ENST00000478761.3:c.114A>T
NM_017519.2:c.2792A>T	NP_059989.2:p.Glu931Val
NM_020732.3:c.2831A>T	NP_065783.3:p.Glu944Val
XM_005267069.3:c.2792A>T	XP_005267126.2:p.Glu931Val
XM_011535984.1:c.1742A>T	XP_011534286.1:p.Glu581Val
XM_011535985.1:c.1562A>T	XP_011534287.1:p.Glu521Val
XM_011535986.1:c.1322A>T	XP_011534288.1:p.Glu441Val
XM_011535987.1:c.941A>T	XP_011534289.1:p.Glu314Val
XM_011535988.1:c.-20+15696A>T	XP_011534290.1:n.-20+15696A>T
NM_001346813.1:c.2792A>T	NP_001333742.1:p.Glu931Val
NM_001363725.1:c.542A>T	NP_001350654.1:p.Glu181Val
XM_011535984.2:c.2873A>T	XP_011534286.2:p.Glu958Val
XM_011535988.3:c.-20+15696A>T	XP_011534290.1:n.-20+15696A>T
XM_017011103.2:c.2873A>T	XP_016866592.1:p.Glu958Val
XM_017011104.1:c.2873A>T	XP_016866593.1:p.Glu958Val
XM_017011105.2:c.2873A>T	XP_016866594.1:p.Glu958Val
XM_017011106.2:c.2873A>T	XP_016866595.1:p.Glu958Val
XM_017011107.2:c.2693A>T	XP_016866596.1:p.Glu898Val
XR_002956289.1:n.2956A>T
NM_001363725.2:c.542A>T	NP_001350654.1:p.Glu181Val
NM_001371656.1:c.3080A>T	NP_001358585.1:p.Glu1027Val
NM_001374820.1:c.3080A>T	NP_001361749.1:p.Glu1027Val
NM_001374828.1:c.3041A>T MANE Select	NP_001361757.1:p.Glu1014Val
NM_017519.3:c.3041A>T	NP_059989.3:p.Glu1014Val