Canonical Allele Identifier: CA460496900
Gene: STAR HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.38003549G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.38146031G>C , CM000670.2:g.38146031G>C GRCh38
NC_000008.10:g.38003549G>C , CM000670.1:g.38003549G>C GRCh37
NC_000008.9:g.38122706G>C NCBI36
NG_011827.1:g.10052C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000276449.9:c.582C>G MANE Select ENSP00000276449.3:p.Gly194=
ENST00000276449.8:c.582C>G ENSP00000276449.3:p.Gly194=
ENST00000520114.1:n.1069C>G
ENST00000522050.1:c.518C>G
NM_000349.2:c.582C>G NP_000340.2:p.Gly194=
XM_006716392.1:c.582C>G XP_006716455.1:p.Gly194=
NM_000349.3:c.582C>G MANE Select NP_000340.2:p.Gly194=
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