Canonical Allele Identifier: CA1381558891

Gene: CHMP2B

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.87254448A= , CM000665.2:g.87254448A=	GRCh38
NC_000003.11:g.87303598A= , CM000665.1:g.87303598A=	GRCh37
NC_000003.10:g.87386288A=	NCBI36
NG_007885.1:g.32186A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263780.9:c.*626A= MANE Select	ENSP00000263780.4:n.*626A=
ENST00000472024.3:c.*626A=	ENSP00000480032.2:n.*626A=
ENST00000676705.1:c.*626A=	ENSP00000504098.1:n.*626A=
ENST00000677929.1:n.4932A=
ENST00000678859.1:n.5017A=
ENST00000263780.8:c.*626A=	ENSP00000263780.4:n.*626A=
ENST00000471660.5:c.*626A=	ENSP00000419998.1:n.*626A=
NM_001244644.1:c.*626A=	NP_001231573.1:n.*626A=
NM_014043.3:c.*626A=	NP_054762.2:n.*626A=
XM_011533576.1:c.*626A=	XP_011531878.1:n.*626A=
XM_011533576.2:c.*626A=	XP_011531878.1:n.*626A=
NM_014043.4:c.*626A= MANE Select	NP_054762.2:n.*626A=
NM_001244644.2:c.*626A=	NP_001231573.1:n.*626A=