Canonical Allele Identifier: CA1777411281
Gene: STAR HGNC NCBI

Linked Data

dbSNP Id: rs956165018
gnomAD v4: 8-38146220-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.38146220C>G , CM000670.2:g.38146220C>G GRCh38
NC_000008.10:g.38003738C>G , CM000670.1:g.38003738C>G GRCh37
NC_000008.9:g.38122895C>G NCBI36
NG_011827.1:g.9863G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000276449.9:c.465+69G>C MANE Select ENSP00000276449.3:n.465+69G>C
ENST00000276449.8:c.465+69G>C ENSP00000276449.3:n.465+69G>C
ENST00000520114.1:n.952+69G>C
ENST00000522050.1:c.401+69G>C
NM_000349.2:c.465+69G>C NP_000340.2:n.465+69G>C
XM_006716392.1:c.465+69G>C XP_006716455.1:n.465+69G>C
NM_000349.3:c.465+69G>C MANE Select NP_000340.2:n.465+69G>C
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