Canonical Allele Identifier: CA460374922
Gene: STAR HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.38001815G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.38144297G>A , CM000670.2:g.38144297G>A GRCh38
NC_000008.10:g.38001815G>A , CM000670.1:g.38001815G>A GRCh37
NC_000008.9:g.38120972G>A NCBI36
NG_011827.1:g.11786C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000276449.9:c.834C>T MANE Select ENSP00000276449.3:p.His278=
ENST00000276449.8:c.834C>T ENSP00000276449.3:p.His278=
ENST00000520114.1:n.2803C>T
ENST00000522050.1:c.676C>T
NM_000349.2:c.834C>T NP_000340.2:p.His278=
XM_006716392.1:c.740C>T XP_006716455.1:p.Thr247Ile
NM_000349.3:c.834C>T MANE Select NP_000340.2:p.His278=
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