Canonical Allele Identifier: CA370695776
Gene: STAR HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.38001848A>T (hg19) chr8:g.38144330A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.38144330A>T , CM000670.2:g.38144330A>T GRCh38
NC_000008.10:g.38001848A>T , CM000670.1:g.38001848A>T GRCh37
NC_000008.9:g.38121005A>T NCBI36
NG_011827.1:g.11753T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000276449.9:c.801T>A MANE Select ENSP00000276449.3:p.Phe267Leu
ENST00000276449.8:c.801T>A ENSP00000276449.3:p.Phe267Leu
ENST00000520114.1:n.2770T>A
ENST00000522050.1:c.643T>A
NM_000349.2:c.801T>A NP_000340.2:p.Phe267Leu
XM_006716392.1:c.707T>A XP_006716455.1:p.Leu236Ter
NM_000349.3:c.801T>A MANE Select NP_000340.2:p.Phe267Leu
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