Canonical Allele Identifier: CA1381558072

Gene: CHMP2B

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.87253472C= , CM000665.2:g.87253472C=	GRCh38
NC_000003.11:g.87302622C= , CM000665.1:g.87302622C=	GRCh37
NC_000003.10:g.87385312C=	NCBI36
NG_007885.1:g.31210C=

Transcript Alleles

HGVS	Amino-acid Change
NM_014043.4:c.493C= MANE Select	NP_054762.2:p.Gln165=
ENST00000263780.9:c.493C= MANE Select	ENSP00000263780.4:p.Gln165=
NM_001244644.1:c.370C=	NP_001231573.1:p.Gln124=
NM_001244644.2:c.370C=	NP_001231573.1:p.Gln124=
NM_014043.3:c.493C=	NP_054762.2:p.Gln165=
ENST00000263780.8:c.493C=	ENSP00000263780.4:p.Gln165=
ENST00000466696.1:n.424C=
ENST00000471660.5:c.370C=	ENSP00000419998.1:p.Gln124=
ENST00000472024.3:c.541C=	ENSP00000480032.2:p.Gln181=
ENST00000494980.5:c.403C=	ENSP00000418920.1:p.Gln135=
ENST00000676705.1:c.541C=	ENSP00000504098.1:p.Gln181=
ENST00000677929.1:n.4157C=
ENST00000678859.1:n.4242C=
XM_011533576.1:c.541C=	XP_011531878.1:p.Gln181=
XM_011533576.2:c.541C=	XP_011531878.1:p.Gln181=