Canonical Allele Identifier: CA460374957
Gene: STAR HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.38001866G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.38144348G>C , CM000670.2:g.38144348G>C GRCh38
NC_000008.10:g.38001866G>C , CM000670.1:g.38001866G>C GRCh37
NC_000008.9:g.38121023G>C NCBI36
NG_011827.1:g.11735C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000276449.9:c.783C>G MANE Select ENSP00000276449.3:p.Ser261=
ENST00000276449.8:c.783C>G ENSP00000276449.3:p.Ser261=
ENST00000520114.1:n.2752C>G
ENST00000522050.1:c.625C>G
NM_000349.2:c.783C>G NP_000340.2:p.Ser261=
XM_006716392.1:c.689C>G XP_006716455.1:p.Pro230Arg
NM_000349.3:c.783C>G MANE Select NP_000340.2:p.Ser261=