Canonical Allele Identifier: CA370699635
Gene: STAR HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.38003628T>G (hg19) chr8:g.38146110T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.38146110T>G , CM000670.2:g.38146110T>G GRCh38
NC_000008.10:g.38003628T>G , CM000670.1:g.38003628T>G GRCh37
NC_000008.9:g.38122785T>G NCBI36
NG_011827.1:g.9973A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000276449.9:c.503A>C MANE Select ENSP00000276449.3:p.His168Pro
ENST00000276449.8:c.503A>C ENSP00000276449.3:p.His168Pro
ENST00000520114.1:n.990A>C
ENST00000522050.1:c.439A>C
NM_000349.2:c.503A>C NP_000340.2:p.His168Pro
XM_006716392.1:c.503A>C XP_006716455.1:p.His168Pro
NM_000349.3:c.503A>C MANE Select NP_000340.2:p.His168Pro
Search 100 bp 5'
Search 100 bp 3'