Canonical Allele Identifier: CA1914325176

Gene: ARID5B

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.61958447A= , CM000672.2:g.61958447A=	GRCh38
NC_000010.10:g.63718206A= , CM000672.1:g.63718206A=	GRCh37
NC_000010.9:g.63388212A=	NCBI36
NG_030027.1:g.62194A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279873.12:c.502+18039A= MANE Select	ENSP00000279873.7:n.502+18039A=
ENST00000644638.1:c.502+18039A=	ENSP00000494412.1:n.502+18039A=
ENST00000681100.1:c.502+18039A=	ENSP00000506119.1:n.502+18039A=
ENST00000279873.11:c.502+18039A=	ENSP00000279873.7:n.502+18039A=
NM_032199.2:c.502+18039A=	NP_115575.1:n.502+18039A=
XM_011540262.1:c.502+18039A=	XP_011538564.1:n.502+18039A=
XM_024448230.1:c.-66+18039A=	XP_024303998.1:n.-66+18039A=
NM_032199.3:c.502+18039A= MANE Select	NP_115575.1:n.502+18039A=