Canonical Allele Identifier: CA4066732

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.156779017C>T , CM000668.2:g.156779017C>T	GRCh38
NC_000006.11:g.157100151C>T , CM000668.1:g.157100151C>T	GRCh37
NC_000006.10:g.157141843C>T	NCBI36
NG_032093.1:g.6088C>T
NG_032093.2:g.6088C>T
NG_066624.1:g.7992C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001374828.1:c.1337C>T MANE Select	NP_001361757.1:p.Ala446Val
ENST00000636930.2:c.1337C>T MANE Select	ENSP00000490491.2:p.Ala446Val
NM_001346813.1:c.1088C>T	NP_001333742.1:p.Ala363Val
NM_001371656.1:c.1337C>T	NP_001358585.1:p.Ala446Val
NM_001374820.1:c.1337C>T	NP_001361749.1:p.Ala446Val
NM_017519.2:c.1088C>T	NP_059989.2:p.Ala363Val
NM_017519.3:c.1337C>T	NP_059989.3:p.Ala446Val
NM_020732.3:c.1088C>T	NP_065783.3:p.Ala363Val
ENST00000346085.10:c.1337C>T	ENSP00000344546.5:p.Ala446Val
ENST00000346085.9:c.1088C>T	ENSP00000344546.4:p.Ala363Val
ENST00000350026.10:c.1088C>T	ENSP00000055163.7:p.Ala363Val
ENST00000350026.11:c.1337C>T	ENSP00000055163.8:p.Ala446Val
ENST00000350026.9:c.1088C>T	ENSP00000055163.7:p.Ala363Val
ENST00000414678.8:c.1337C>T	ENSP00000412835.3:p.Ala446Val
ENST00000637015.2:c.1337C>T	ENSP00000489729.2:p.Ala446Val
ENST00000647938.1:c.1088C>T	ENSP00000498155.1:p.Ala363Val
ENST00000674190.1:n.44C>T
ENST00000674298.1:c.1077C>T
XM_005267069.3:c.1088C>T	XP_005267126.2:p.Ala363Val
XM_011535984.1:c.-44C>T	XP_011534286.1:n.-44C>T
XM_011535984.2:c.1088C>T	XP_011534286.2:p.Ala363Val
XM_011535985.1:c.-44C>T	XP_011534287.1:n.-44C>T
XM_017011103.2:c.1088C>T	XP_016866592.1:p.Ala363Val
XM_017011104.1:c.1088C>T	XP_016866593.1:p.Ala363Val
XM_017011105.2:c.1088C>T	XP_016866594.1:p.Ala363Val
XM_017011106.2:c.1088C>T	XP_016866595.1:p.Ala363Val
XM_017011107.2:c.1088C>T	XP_016866596.1:p.Ala363Val
XR_002956289.1:n.1171C>T