Canonical Allele Identifier: CA370695680
Gene: STAR HGNC NCBI

Linked Data

gnomAD v4: 8-38144316-C-G
MyVariant Identifiers: chr8:g.38001834C>G (hg19) chr8:g.38144316C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.38144316C>G , CM000670.2:g.38144316C>G GRCh38
NC_000008.10:g.38001834C>G , CM000670.1:g.38001834C>G GRCh37
NC_000008.9:g.38120991C>G NCBI36
NG_011827.1:g.11767G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000276449.9:c.815G>C MANE Select ENSP00000276449.3:p.Arg272Pro
ENST00000276449.8:c.815G>C ENSP00000276449.3:p.Arg272Pro
ENST00000520114.1:n.2784G>C
ENST00000522050.1:c.657G>C
NM_000349.2:c.815G>C NP_000340.2:p.Arg272Pro
XM_006716392.1:c.721G>C XP_006716455.1:p.Ala241Pro
NM_000349.3:c.815G>C MANE Select NP_000340.2:p.Arg272Pro
Search 100 bp 5'
Search 100 bp 3'