Canonical Allele Identifier: CA1381535229

Gene: CHMP2B

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.87227421C= , CM000665.2:g.87227421C=	GRCh38
NC_000003.11:g.87276571C= , CM000665.1:g.87276571C=	GRCh37
NC_000003.10:g.87359261C=	NCBI36
NG_007885.1:g.5159C=

Transcript Alleles

HGVS	Amino-acid Change
NM_014043.4:c.-102C= MANE Select	NP_054762.2:n.-102C=
ENST00000263780.9:c.-102C= MANE Select	ENSP00000263780.4:n.-102C=
NM_001244644.1:c.-133C=	NP_001231573.1:n.-133C=
NM_001244644.2:c.-133C=	NP_001231573.1:n.-133C=
NM_014043.3:c.-102C=	NP_054762.2:n.-102C=
ENST00000263780.8:c.-102C=	ENSP00000263780.4:n.-102C=
ENST00000471660.5:c.-133C=	ENSP00000419998.1:n.-133C=
ENST00000472024.2:c.-185C=	ENSP00000480032.1:n.-185C=
ENST00000472024.3:c.-185C=	ENSP00000480032.2:n.-185C=
ENST00000494980.5:c.-102C=	ENSP00000418920.1:n.-102C=
ENST00000676705.1:c.-181C=	ENSP00000504098.1:n.-181C=
ENST00000676947.1:n.52C=
ENST00000677929.1:n.137C=
ENST00000678859.1:n.95C=