Canonical Allele Identifier: CA1381547719

Gene: CHMP2B

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.87240749A= , CM000665.2:g.87240749A=	GRCh38
NC_000003.11:g.87289899A= , CM000665.1:g.87289899A=	GRCh37
NC_000003.10:g.87372589A=	NCBI36
NG_007885.1:g.18487A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263780.9:c.85A= MANE Select	ENSP00000263780.4:p.Ile29=
ENST00000472024.3:c.133A=	ENSP00000480032.2:p.Ile45=
ENST00000676705.1:c.133A=	ENSP00000504098.1:p.Ile45=
ENST00000676947.1:n.238A=
ENST00000677929.1:n.323A=
ENST00000678818.1:n.1062+296A=
ENST00000678859.1:n.408A=
ENST00000263780.8:c.85A=	ENSP00000263780.4:p.Ile29=
ENST00000471660.5:c.4-4965A=	ENSP00000419998.1:n.4-4965A=
ENST00000472024.2:c.133A=	ENSP00000480032.1:p.Ile45=
ENST00000494980.5:c.85A=	ENSP00000418920.1:p.Ile29=
NM_001244644.1:c.4-4965A=	NP_001231573.1:n.4-4965A=
NM_014043.3:c.85A=	NP_054762.2:p.Ile29=
XM_011533576.1:c.133A=	XP_011531878.1:p.Ile45=
XM_011533576.2:c.133A=	XP_011531878.1:p.Ile45=
NM_014043.4:c.85A= MANE Select	NP_054762.2:p.Ile29=
NM_001244644.2:c.4-4965A=	NP_001231573.1:n.4-4965A=