Canonical Allele Identifier: CA1675517052

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148869C= , CM000668.2:g.157148869C=	GRCh38
NC_000006.11:g.157470003C= , CM000668.1:g.157470003C=	GRCh37
NC_000006.10:g.157511695C=	NCBI36
NG_032093.1:g.375940C=
NG_032093.2:g.375940C=
NG_066624.1:g.377844C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3007C=	ENSP00000055163.8:p.Pro1003=
ENST00000414678.8:c.2917C=	ENSP00000412835.3:p.Pro973=
ENST00000637015.2:c.3007C=	ENSP00000489729.2:p.Pro1003=
ENST00000319584.11:c.1021C=	ENSP00000313006.7:p.Pro341=
ENST00000346085.10:c.3046C=	ENSP00000344546.5:p.Pro1016=
ENST00000350026.10:c.2758C=	ENSP00000055163.7:p.Pro920=
ENST00000414678.7:c.1165C=	ENSP00000412835.2:p.Pro389=
ENST00000452544.2:n.908C=
ENST00000635849.1:c.328C=	ENSP00000490948.1:p.Pro110=
ENST00000636426.1:n.141C=
ENST00000636930.2:c.3007C= MANE Select	ENSP00000490491.2:p.Pro1003=
ENST00000637015.1:c.246C=
ENST00000637568.1:c.50C=
ENST00000637810.1:c.508C=	ENSP00000489636.1:p.Pro170=
ENST00000637904.1:c.508C=	ENSP00000490550.1:p.Pro170=
ENST00000647938.1:c.2797C=	ENSP00000498155.1:p.Pro933=
ENST00000674190.1:n.1756C=
ENST00000319584.10:c.1024C=	ENSP00000313006.6:p.Pro342=
ENST00000346085.9:c.2797C=	ENSP00000344546.4:p.Pro933=
ENST00000350026.9:c.2758C=	ENSP00000055163.7:p.Pro920=
ENST00000414678.6:c.1165C=	ENSP00000412835.2:p.Pro389=
ENST00000452544.1:n.854C=
ENST00000478761.3:c.80C=
NM_017519.2:c.2758C=	NP_059989.2:p.Pro920=
NM_020732.3:c.2797C=	NP_065783.3:p.Pro933=
XM_005267069.3:c.2758C=	XP_005267126.2:p.Pro920=
XM_011535984.1:c.1708C=	XP_011534286.1:p.Pro570=
XM_011535985.1:c.1528C=	XP_011534287.1:p.Pro510=
XM_011535986.1:c.1288C=	XP_011534288.1:p.Pro430=
XM_011535987.1:c.907C=	XP_011534289.1:p.Pro303=
XM_011535988.1:c.-20+15662C=	XP_011534290.1:n.-20+15662C=
NM_001346813.1:c.2758C=	NP_001333742.1:p.Pro920=
NM_001363725.1:c.508C=	NP_001350654.1:p.Pro170=
XM_011535984.2:c.2839C=	XP_011534286.2:p.Pro947=
XM_011535988.3:c.-20+15662C=	XP_011534290.1:n.-20+15662C=
XM_017011103.2:c.2839C=	XP_016866592.1:p.Pro947=
XM_017011104.1:c.2839C=	XP_016866593.1:p.Pro947=
XM_017011105.2:c.2839C=	XP_016866594.1:p.Pro947=
XM_017011106.2:c.2839C=	XP_016866595.1:p.Pro947=
XM_017011107.2:c.2659C=	XP_016866596.1:p.Pro887=
XR_002956289.1:n.2922C=
NM_001363725.2:c.508C=	NP_001350654.1:p.Pro170=
NM_001371656.1:c.3046C=	NP_001358585.1:p.Pro1016=
NM_001374820.1:c.3046C=	NP_001361749.1:p.Pro1016=
NM_001374828.1:c.3007C= MANE Select	NP_001361757.1:p.Pro1003=
NM_017519.3:c.3007C=	NP_059989.3:p.Pro1003=