Canonical Allele Identifier: CA658821506
Gene: STAR HGNC NCBI

Linked Data

ClinVar Variation Id: 557765
ClinVar RCV Id: RCV000673944
dbSNP Id: rs1053284504
MyVariant Identifiers: chr8:g.38003676A>T (hg19) chr8:g.38146158A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.38146158A>T , CM000670.2:g.38146158A>T GRCh38
NC_000008.10:g.38003676A>T , CM000670.1:g.38003676A>T GRCh37
NC_000008.9:g.38122833A>T NCBI36
NG_011827.1:g.9925T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000276449.9:c.466-11T>A MANE Select ENSP00000276449.3:n.466-11T>A
ENST00000276449.8:c.466-11T>A ENSP00000276449.3:n.466-11T>A
ENST00000520114.1:n.953-11T>A
ENST00000522050.1:c.402-11T>A
NM_000349.2:c.466-11T>A NP_000340.2:n.466-11T>A
XM_006716392.1:c.466-11T>A XP_006716455.1:n.466-11T>A
NM_000349.3:c.466-11T>A MANE Select NP_000340.2:n.466-11T>A
Search 100 bp 5'
Search 100 bp 3'