Canonical Allele Identifier: CA1914338209

Gene: ARID5B

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.61987994T= , CM000672.2:g.61987994T=	GRCh38
NC_000010.10:g.63747753T= , CM000672.1:g.63747753T=	GRCh37
NC_000010.9:g.63417759T=	NCBI36
NG_030027.1:g.91741T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000279873.12:c.503-12097T= MANE Select	ENSP00000279873.7:n.503-12097T=
ENST00000644638.1:c.503-12097T=	ENSP00000494412.1:n.503-12097T=
ENST00000681100.1:c.503-12097T=	ENSP00000506119.1:n.503-12097T=
ENST00000279873.11:c.503-12097T=	ENSP00000279873.7:n.503-12097T=
NM_032199.2:c.503-12097T=	NP_115575.1:n.503-12097T=
XM_011540262.1:c.502+47586T=	XP_011538564.1:n.502+47586T=
XM_024448230.1:c.-65-12097T=	XP_024303998.1:n.-65-12097T=
NM_032199.3:c.503-12097T= MANE Select	NP_115575.1:n.503-12097T=