Canonical Allele Identifier: CA1381535122

Gene: CHMP2B

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.87227327G= , CM000665.2:g.87227327G=	GRCh38
NC_000003.11:g.87276477G= , CM000665.1:g.87276477G=	GRCh37
NC_000003.10:g.87359167G=	NCBI36
NG_007885.1:g.5065G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000263780.9:c.-196G= MANE Select	ENSP00000263780.4:n.-196G=
ENST00000472024.3:c.-279G=	ENSP00000480032.2:n.-279G=
ENST00000676705.1:c.-275G=	ENSP00000504098.1:n.-275G=
ENST00000677929.1:n.43G=
ENST00000678859.1:n.1G=
ENST00000263780.8:c.-196G=	ENSP00000263780.4:n.-196G=
ENST00000471660.5:c.-227G=	ENSP00000419998.1:n.-227G=
ENST00000472024.2:c.-279G=	ENSP00000480032.1:n.-279G=
ENST00000494980.5:c.-196G=	ENSP00000418920.1:n.-196G=
NM_001244644.1:c.-227G=	NP_001231573.1:n.-227G=
NM_014043.3:c.-196G=	NP_054762.2:n.-196G=
NM_014043.4:c.-196G= MANE Select	NP_054762.2:n.-196G=
NM_001244644.2:c.-227G=	NP_001231573.1:n.-227G=