Canonical Allele Identifier: CA1381535120

Gene: CHMP2B

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.87227325C= , CM000665.2:g.87227325C=	GRCh38
NC_000003.11:g.87276475C= , CM000665.1:g.87276475C=	GRCh37
NC_000003.10:g.87359165C=	NCBI36
NG_007885.1:g.5063C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000263780.9:c.-198C= MANE Select	ENSP00000263780.4:n.-198C=
ENST00000472024.3:c.-281C=	ENSP00000480032.2:n.-281C=
ENST00000676705.1:c.-277C=	ENSP00000504098.1:n.-277C=
ENST00000677929.1:n.41C=
ENST00000263780.8:c.-198C=	ENSP00000263780.4:n.-198C=
ENST00000471660.5:c.-229C=	ENSP00000419998.1:n.-229C=
ENST00000472024.2:c.-281C=	ENSP00000480032.1:n.-281C=
ENST00000494980.5:c.-198C=	ENSP00000418920.1:n.-198C=
NM_001244644.1:c.-229C=	NP_001231573.1:n.-229C=
NM_014043.3:c.-198C=	NP_054762.2:n.-198C=
NM_014043.4:c.-198C= MANE Select	NP_054762.2:n.-198C=
NM_001244644.2:c.-229C=	NP_001231573.1:n.-229C=