Canonical Allele Identifier: CA370695634
Gene: STAR HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.38001822T>G (hg19) chr8:g.38144304T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.38144304T>G , CM000670.2:g.38144304T>G GRCh38
NC_000008.10:g.38001822T>G , CM000670.1:g.38001822T>G GRCh37
NC_000008.9:g.38120979T>G NCBI36
NG_011827.1:g.11779A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000276449.9:c.827A>C MANE Select ENSP00000276449.3:p.Glu276Ala
ENST00000276449.8:c.827A>C ENSP00000276449.3:p.Glu276Ala
ENST00000520114.1:n.2796A>C
ENST00000522050.1:c.669A>C
NM_000349.2:c.827A>C NP_000340.2:p.Glu276Ala
XM_006716392.1:c.733A>C XP_006716455.1:p.Ser245Arg
NM_000349.3:c.827A>C MANE Select NP_000340.2:p.Glu276Ala
Search 100 bp 5'
Search 100 bp 3'