Canonical Allele Identifier: CA1381558918

Gene: CHMP2B

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.87254481A= , CM000665.2:g.87254481A=	GRCh38
NC_000003.11:g.87303631A= , CM000665.1:g.87303631A=	GRCh37
NC_000003.10:g.87386321A=	NCBI36
NG_007885.1:g.32219A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263780.9:c.*659A= MANE Select	ENSP00000263780.4:n.*659A=
ENST00000472024.3:c.*659A=	ENSP00000480032.2:n.*659A=
ENST00000676705.1:c.*659A=	ENSP00000504098.1:n.*659A=
ENST00000677929.1:n.4965A=
ENST00000678859.1:n.5050A=
ENST00000263780.8:c.*659A=	ENSP00000263780.4:n.*659A=
ENST00000471660.5:c.*659A=	ENSP00000419998.1:n.*659A=
NM_001244644.1:c.*659A=	NP_001231573.1:n.*659A=
NM_014043.3:c.*659A=	NP_054762.2:n.*659A=
XM_011533576.1:c.*659A=	XP_011531878.1:n.*659A=
XM_011533576.2:c.*659A=	XP_011531878.1:n.*659A=
NM_014043.4:c.*659A= MANE Select	NP_054762.2:n.*659A=
NM_001244644.2:c.*659A=	NP_001231573.1:n.*659A=