Canonical Allele Identifier: CA434576674

Gene: CHMP2B

Linked Data

• MyVariant Identifiers: chr3:g.87302585T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.87253435T>A , CM000665.2:g.87253435T>A	GRCh38
NC_000003.11:g.87302585T>A , CM000665.1:g.87302585T>A	GRCh37
NC_000003.10:g.87385275T>A	NCBI36
NG_007885.1:g.31173T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000263780.9:c.456T>A MANE Select	ENSP00000263780.4:p.Gly152=
ENST00000472024.3:c.504T>A	ENSP00000480032.2:p.Gly168=
ENST00000676705.1:c.504T>A	ENSP00000504098.1:p.Gly168=
ENST00000677929.1:n.4120T>A
ENST00000678859.1:n.4205T>A
ENST00000263780.8:c.456T>A	ENSP00000263780.4:p.Gly152=
ENST00000466696.1:n.387T>A
ENST00000471660.5:c.333T>A	ENSP00000419998.1:p.Gly111=
ENST00000472024.2:c.504T>A	ENSP00000480032.1:p.Gly168=
ENST00000494980.5:c.366T>A	ENSP00000418920.1:p.Gly122=
NM_001244644.1:c.333T>A	NP_001231573.1:p.Gly111=
NM_014043.3:c.456T>A	NP_054762.2:p.Gly152=
XM_011533576.1:c.504T>A	XP_011531878.1:p.Gly168=
XM_011533576.2:c.504T>A	XP_011531878.1:p.Gly168=
NM_014043.4:c.456T>A MANE Select	NP_054762.2:p.Gly152=
NM_001244644.2:c.333T>A	NP_001231573.1:p.Gly111=