Canonical Allele Identifier: CA370698897
Gene: STAR HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.38003514A>T (hg19) chr8:g.38145996A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.38145996A>T , CM000670.2:g.38145996A>T GRCh38
NC_000008.10:g.38003514A>T , CM000670.1:g.38003514A>T GRCh37
NC_000008.9:g.38122671A>T NCBI36
NG_011827.1:g.10087T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000276449.9:c.617T>A MANE Select ENSP00000276449.3:p.Phe206Tyr
ENST00000276449.8:c.617T>A ENSP00000276449.3:p.Phe206Tyr
ENST00000520114.1:n.1104T>A
ENST00000522050.1:c.553T>A
NM_000349.2:c.617T>A NP_000340.2:p.Phe206Tyr
XM_006716392.1:c.617T>A XP_006716455.1:p.Phe206Tyr
NM_000349.3:c.617T>A MANE Select NP_000340.2:p.Phe206Tyr
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