Canonical Allele Identifier: CA114744
Gene: CHMP4B HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 1086
ClinVar RCV Id: RCV000001144
dbSNP Id: rs118203966

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33851064G>A , CM000682.2:g.33851064G>A GRCh38
NC_000020.9:g.31902531G>A NCBI36
NC_000020.10:g.32438870G>A , CM000682.1:g.32438870G>A GRCh37
NG_015820.1:g.44761G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000217402.2:c.481G>A ENSP00000217402.2:p.Glu161Lys
NM_176812.4:c.481G>A NP_789782.1:p.Glu161Lys