Canonical Allele Identifier: CA460374955
Gene: STAR HGNC NCBI

Linked Data

gnomAD v4: 8-38144345-C-T
MyVariant Identifiers: chr8:g.38001863C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.38144345C>T , CM000670.2:g.38144345C>T GRCh38
NC_000008.10:g.38001863C>T , CM000670.1:g.38001863C>T GRCh37
NC_000008.9:g.38121020C>T NCBI36
NG_011827.1:g.11738G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000276449.9:c.786G>A MANE Select ENSP00000276449.3:p.Gln262=
ENST00000276449.8:c.786G>A ENSP00000276449.3:p.Gln262=
ENST00000520114.1:n.2755G>A
ENST00000522050.1:c.628G>A
NM_000349.2:c.786G>A NP_000340.2:p.Gln262=
XM_006716392.1:c.692G>A XP_006716455.1:p.Arg231Lys
NM_000349.3:c.786G>A MANE Select NP_000340.2:p.Gln262=
Search 100 bp 5'
Search 100 bp 3'