Canonical Allele Identifier: CA120040
Gene: STAR HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 8993
ClinVar RCV Id: RCV000009556
dbSNP Id: rs137852690

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.38145313G>A , CM000670.2:g.38145313G>A GRCh38
NC_000008.10:g.38002831G>A , CM000670.1:g.38002831G>A GRCh37
NC_000008.9:g.38121988G>A NCBI36
NG_011827.1:g.10770C>T

Transcript Alleles

HGVS Amino-acid change
NM_000349.2:c.653C>T VV NP_000340.2:p.Ala218Val
XM_006716392.1:c.650+650C>T XP_006716455.1:p.=
ENST00000276449.8:c.653C>T ENSP00000276449.3:p.Ala218Val
ENST00000520114.1:n.1787C>T
ENST00000522050.1:n.586+650C>T