Canonical Allele Identifier: CA1675523527

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201385C= , CM000668.2:g.157201385C=	GRCh38
NC_000006.11:g.157522519C= , CM000668.1:g.157522519C=	GRCh37
NC_000006.10:g.157564211C=	NCBI36
NG_032093.1:g.428456C=
NG_032093.2:g.428456C=
NG_066624.1:g.430360C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.5001C=	ENSP00000055163.8:p.Pro1667=
ENST00000414678.8:c.5070C=	ENSP00000412835.3:p.Pro1690=
ENST00000637015.2:c.5289C=	ENSP00000489729.2:p.Pro1763=
ENST00000346085.10:c.5040C=	ENSP00000344546.5:p.Pro1680=
ENST00000350026.10:c.4752C=	ENSP00000055163.7:p.Pro1584=
ENST00000414678.7:c.3318C=	ENSP00000412835.2:p.Pro1106=
ENST00000635849.1:c.2481C=	ENSP00000490948.1:p.Pro827=
ENST00000635957.1:c.2112C=	ENSP00000490385.1:p.Pro704=
ENST00000636227.1:n.3623C=
ENST00000636254.1:n.1080C=
ENST00000636930.2:c.5160C= MANE Select	ENSP00000490491.2:p.Pro1720=
ENST00000636940.1:n.3157C=
ENST00000637015.1:c.2528C=
ENST00000637568.1:c.2442C=
ENST00000637741.1:n.1826C=
ENST00000637810.1:c.2502C=	ENSP00000489636.1:p.Pro834=
ENST00000637904.1:c.2661C=	ENSP00000490550.1:p.Pro887=
ENST00000647938.1:c.4791C=	ENSP00000498155.1:p.Pro1597=
ENST00000346085.9:c.4791C=	ENSP00000344546.4:p.Pro1597=
ENST00000350026.9:c.4752C=	ENSP00000055163.7:p.Pro1584=
ENST00000414678.6:c.3318C=	ENSP00000412835.2:p.Pro1106=
NM_017519.2:c.4752C=	NP_059989.2:p.Pro1584=
NM_020732.3:c.4791C=	NP_065783.3:p.Pro1597=
XM_005267069.3:c.4911C=	XP_005267126.2:p.Pro1637=
XM_011535984.1:c.3990C=	XP_011534286.1:p.Pro1330=
XM_011535985.1:c.3810C=	XP_011534287.1:p.Pro1270=
XM_011535986.1:c.3570C=	XP_011534288.1:p.Pro1190=
XM_011535987.1:c.3189C=	XP_011534289.1:p.Pro1063=
XM_011535988.1:c.2052C=	XP_011534290.1:p.Pro684=
NM_001346813.1:c.4911C=	NP_001333742.1:p.Pro1637=
NM_001363725.1:c.2661C=	NP_001350654.1:p.Pro887=
XM_011535984.2:c.5121C=	XP_011534286.2:p.Pro1707=
XM_011535988.3:c.2052C=	XP_011534290.1:p.Pro684=
XM_017011103.2:c.5022C=	XP_016866592.1:p.Pro1674=
XM_017011104.1:c.4992C=	XP_016866593.1:p.Pro1664=
XM_017011105.2:c.4962C=	XP_016866594.1:p.Pro1654=
XM_017011106.2:c.4833C=	XP_016866595.1:p.Pro1611=
XM_017011107.2:c.4812C=	XP_016866596.1:p.Pro1604=
XR_002956289.1:n.5107C=
NM_001363725.2:c.2661C=	NP_001350654.1:p.Pro887=
NM_001371656.1:c.5040C=	NP_001358585.1:p.Pro1680=
NM_001374820.1:c.5040C=	NP_001361749.1:p.Pro1680=
NM_001374828.1:c.5160C= MANE Select	NP_001361757.1:p.Pro1720=
NM_017519.3:c.5001C=	NP_059989.3:p.Pro1667=