Canonical Allele Identifier: CA460375045
Gene: STAR HGNC NCBI

Linked Data

dbSNP Id: rs552623910
MyVariant Identifiers: chr8:g.38003489A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.38145971A>C , CM000670.2:g.38145971A>C GRCh38
NC_000008.10:g.38003489A>C , CM000670.1:g.38003489A>C GRCh37
NC_000008.9:g.38122646A>C NCBI36
NG_011827.1:g.10112T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000276449.9:c.642T>G MANE Select ENSP00000276449.3:p.Gly214=
ENST00000276449.8:c.642T>G ENSP00000276449.3:p.Gly214=
ENST00000520114.1:n.1129T>G
ENST00000522050.1:c.578T>G
NM_000349.2:c.642T>G NP_000340.2:p.Gly214=
XM_006716392.1:c.642T>G XP_006716455.1:p.Gly214=
NM_000349.3:c.642T>G MANE Select NP_000340.2:p.Gly214=
Search 100 bp 5'
Search 100 bp 3'