Canonical Allele Identifier: CA1381558311

Gene: CHMP2B

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.87253736C= , CM000665.2:g.87253736C=	GRCh38
NC_000003.11:g.87302886C= , CM000665.1:g.87302886C=	GRCh37
NC_000003.10:g.87385576C=	NCBI36
NG_007885.1:g.31474C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263780.9:c.556C= MANE Select	ENSP00000263780.4:p.Arg186=
ENST00000472024.3:c.604C=	ENSP00000480032.2:p.Arg202=
ENST00000676705.1:c.604C=	ENSP00000504098.1:p.Arg202=
ENST00000677929.1:n.4220C=
ENST00000678859.1:n.4305C=
ENST00000263780.8:c.556C=	ENSP00000263780.4:p.Arg186=
ENST00000466696.1:n.487C=
ENST00000471660.5:c.433C=	ENSP00000419998.1:p.Arg145=
ENST00000494980.5:c.466C=	ENSP00000418920.1:p.Arg156=
NM_001244644.1:c.433C=	NP_001231573.1:p.Arg145=
NM_014043.3:c.556C=	NP_054762.2:p.Arg186=
XM_011533576.1:c.604C=	XP_011531878.1:p.Arg202=
XM_011533576.2:c.604C=	XP_011531878.1:p.Arg202=
NM_014043.4:c.556C= MANE Select	NP_054762.2:p.Arg186=
NM_001244644.2:c.433C=	NP_001231573.1:p.Arg145=