Canonical Allele Identifier: CA460496838
Gene: STAR HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.38003498C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.38145980C>T , CM000670.2:g.38145980C>T GRCh38
NC_000008.10:g.38003498C>T , CM000670.1:g.38003498C>T GRCh37
NC_000008.9:g.38122655C>T NCBI36
NG_011827.1:g.10103G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000276449.9:c.633G>A MANE Select ENSP00000276449.3:p.Glu211=
ENST00000276449.8:c.633G>A ENSP00000276449.3:p.Glu211=
ENST00000520114.1:n.1120G>A
ENST00000522050.1:c.569G>A
NM_000349.2:c.633G>A NP_000340.2:p.Glu211=
XM_006716392.1:c.633G>A XP_006716455.1:p.Glu211=
NM_000349.3:c.633G>A MANE Select NP_000340.2:p.Glu211=