Canonical Allele Identifier: CA911557995

Gene: CHMP2B

Linked Data

• dbSNP Id: rs746713672
• MyVariant Identifiers: chr3:g.87277091A>G (hg19) ; chr3:g.87227941A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.87227941A>G , CM000665.2:g.87227941A>G	GRCh38
NC_000003.11:g.87277091A>G , CM000665.1:g.87277091A>G	GRCh37
NC_000003.10:g.87359781A>G	NCBI36
NG_007885.1:g.5679A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000263780.9:c.34+385A>G MANE Select	ENSP00000263780.4:n.34+385A>G
ENST00000472024.3:c.-50+385A>G	ENSP00000480032.2:n.-50+385A>G
ENST00000676705.1:c.-46+385A>G	ENSP00000504098.1:n.-46+385A>G
ENST00000676947.1:n.187+385A>G
ENST00000677929.1:n.272+385A>G
ENST00000678859.1:n.230+385A>G
ENST00000263780.8:c.34+385A>G	ENSP00000263780.4:n.34+385A>G
ENST00000471660.5:c.3+385A>G	ENSP00000419998.1:n.3+385A>G
ENST00000472024.2:c.-50+385A>G	ENSP00000480032.1:n.-50+385A>G
ENST00000494980.5:c.34+385A>G	ENSP00000418920.1:n.34+385A>G
NM_001244644.1:c.3+385A>G	NP_001231573.1:n.3+385A>G
NM_014043.3:c.34+385A>G	NP_054762.2:n.34+385A>G
NM_014043.4:c.34+385A>G MANE Select	NP_054762.2:n.34+385A>G
NM_001244644.2:c.3+385A>G	NP_001231573.1:n.3+385A>G