Canonical Allele Identifier: CA370699730
Gene: STAR HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.38003649C>G (hg19) chr8:g.38146131C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.38146131C>G , CM000670.2:g.38146131C>G GRCh38
NC_000008.10:g.38003649C>G , CM000670.1:g.38003649C>G GRCh37
NC_000008.9:g.38122806C>G NCBI36
NG_011827.1:g.9952G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000276449.9:c.482G>C MANE Select ENSP00000276449.3:p.Gly161Ala
ENST00000276449.8:c.482G>C ENSP00000276449.3:p.Gly161Ala
ENST00000520114.1:n.969G>C
ENST00000522050.1:c.418G>C
NM_000349.2:c.482G>C NP_000340.2:p.Gly161Ala
XM_006716392.1:c.482G>C XP_006716455.1:p.Gly161Ala
NM_000349.3:c.482G>C MANE Select NP_000340.2:p.Gly161Ala
Search 100 bp 5'
Search 100 bp 3'