Canonical Allele Identifier: CA79035826

Gene: CHMP2B

Linked Data

• dbSNP Id: rs384094
• MyVariant Identifiers: chr3:g.87303586G>A (hg19) ; chr3:g.87254436G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.87254436G>A , CM000665.2:g.87254436G>A	GRCh38
NC_000003.11:g.87303586G>A , CM000665.1:g.87303586G>A	GRCh37
NC_000003.10:g.87386276G>A	NCBI36
NG_007885.1:g.32174G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263780.9:c.*614G>A MANE Select	ENSP00000263780.4:n.*614G>A
ENST00000472024.3:c.*614G>A	ENSP00000480032.2:n.*614G>A
ENST00000676705.1:c.*614G>A	ENSP00000504098.1:n.*614G>A
ENST00000677929.1:n.4920G>A
ENST00000678859.1:n.5005G>A
ENST00000263780.8:c.*614G>A	ENSP00000263780.4:n.*614G>A
ENST00000471660.5:c.*614G>A	ENSP00000419998.1:n.*614G>A
NM_001244644.1:c.*614G>A	NP_001231573.1:n.*614G>A
NM_014043.3:c.*614G>A	NP_054762.2:n.*614G>A
XM_011533576.1:c.*614G>A	XP_011531878.1:n.*614G>A
XM_011533576.2:c.*614G>A	XP_011531878.1:n.*614G>A
NM_014043.4:c.*614G>A MANE Select	NP_054762.2:n.*614G>A
NM_001244644.2:c.*614G>A	NP_001231573.1:n.*614G>A