Canonical Allele Identifier: CA1914327466

Gene: ARID5B

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.61963701A= , CM000672.2:g.61963701A=	GRCh38
NC_000010.10:g.63723460A= , CM000672.1:g.63723460A=	GRCh37
NC_000010.9:g.63393466A=	NCBI36
NG_030027.1:g.67448A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279873.12:c.502+23293A= MANE Select	ENSP00000279873.7:n.502+23293A=
ENST00000644638.1:c.502+23293A=	ENSP00000494412.1:n.502+23293A=
ENST00000681100.1:c.502+23293A=	ENSP00000506119.1:n.502+23293A=
ENST00000279873.11:c.502+23293A=	ENSP00000279873.7:n.502+23293A=
NM_032199.2:c.502+23293A=	NP_115575.1:n.502+23293A=
XM_011540262.1:c.502+23293A=	XP_011538564.1:n.502+23293A=
XM_024448230.1:c.-66+23293A=	XP_024303998.1:n.-66+23293A=
NM_032199.3:c.502+23293A= MANE Select	NP_115575.1:n.502+23293A=