Canonical Allele Identifier: CA1675543069

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200777C= , CM000668.2:g.157200777C=	GRCh38
NC_000006.11:g.157521911C= , CM000668.1:g.157521911C=	GRCh37
NC_000006.10:g.157563603C=	NCBI36
NG_032093.1:g.427848C=
NG_032093.2:g.427848C=
NG_066624.1:g.429752C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4393C=	ENSP00000055163.8:p.Gln1465=
ENST00000414678.8:c.4462C=	ENSP00000412835.3:p.Gln1488=
ENST00000637015.2:c.4681C=	ENSP00000489729.2:p.Gln1561=
ENST00000346085.10:c.4432C=	ENSP00000344546.5:p.Gln1478=
ENST00000350026.10:c.4144C=	ENSP00000055163.7:p.Gln1382=
ENST00000414678.7:c.2710C=	ENSP00000412835.2:p.Gln904=
ENST00000635849.1:c.1873C=	ENSP00000490948.1:p.Gln625=
ENST00000635957.1:c.1504C=	ENSP00000490385.1:p.Gln502=
ENST00000636227.1:n.3015C=
ENST00000636254.1:n.472C=
ENST00000636930.2:c.4552C= MANE Select	ENSP00000490491.2:p.Gln1518=
ENST00000636940.1:n.2549C=
ENST00000637015.1:c.1920C=
ENST00000637568.1:c.1834C=
ENST00000637741.1:n.1218C=
ENST00000637810.1:c.1894C=	ENSP00000489636.1:p.Gln632=
ENST00000637904.1:c.2053C=	ENSP00000490550.1:p.Gln685=
ENST00000647938.1:c.4183C=	ENSP00000498155.1:p.Gln1395=
ENST00000346085.9:c.4183C=	ENSP00000344546.4:p.Gln1395=
ENST00000350026.9:c.4144C=	ENSP00000055163.7:p.Gln1382=
ENST00000414678.6:c.2710C=	ENSP00000412835.2:p.Gln904=
NM_017519.2:c.4144C=	NP_059989.2:p.Gln1382=
NM_020732.3:c.4183C=	NP_065783.3:p.Gln1395=
XM_005267069.3:c.4303C=	XP_005267126.2:p.Gln1435=
XM_011535984.1:c.3382C=	XP_011534286.1:p.Gln1128=
XM_011535985.1:c.3202C=	XP_011534287.1:p.Gln1068=
XM_011535986.1:c.2962C=	XP_011534288.1:p.Gln988=
XM_011535987.1:c.2581C=	XP_011534289.1:p.Gln861=
XM_011535988.1:c.1444C=	XP_011534290.1:p.Gln482=
NM_001346813.1:c.4303C=	NP_001333742.1:p.Gln1435=
NM_001363725.1:c.2053C=	NP_001350654.1:p.Gln685=
XM_011535984.2:c.4513C=	XP_011534286.2:p.Gln1505=
XM_011535988.3:c.1444C=	XP_011534290.1:p.Gln482=
XM_017011103.2:c.4414C=	XP_016866592.1:p.Gln1472=
XM_017011104.1:c.4384C=	XP_016866593.1:p.Gln1462=
XM_017011105.2:c.4354C=	XP_016866594.1:p.Gln1452=
XM_017011106.2:c.4225C=	XP_016866595.1:p.Gln1409=
XM_017011107.2:c.4204C=	XP_016866596.1:p.Gln1402=
XR_002956289.1:n.4499C=
NM_001363725.2:c.2053C=	NP_001350654.1:p.Gln685=
NM_001371656.1:c.4432C=	NP_001358585.1:p.Gln1478=
NM_001374820.1:c.4432C=	NP_001361749.1:p.Gln1478=
NM_001374828.1:c.4552C= MANE Select	NP_001361757.1:p.Gln1518=
NM_017519.3:c.4393C=	NP_059989.3:p.Gln1465=