Canonical Allele Identifier: CA460374915
Gene: STAR HGNC NCBI

Linked Data

gnomAD v4: 8-38144288-A-T
MyVariant Identifiers: chr8:g.38001806A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.38144288A>T , CM000670.2:g.38144288A>T GRCh38
NC_000008.10:g.38001806A>T , CM000670.1:g.38001806A>T GRCh37
NC_000008.9:g.38120963A>T NCBI36
NG_011827.1:g.11795T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000276449.9:c.843T>A MANE Select ENSP00000276449.3:p.Ser281=
ENST00000276449.8:c.843T>A ENSP00000276449.3:p.Ser281=
ENST00000520114.1:n.2812T>A
ENST00000522050.1:c.685T>A
NM_000349.2:c.843T>A NP_000340.2:p.Ser281=
XM_006716392.1:c.749T>A XP_006716455.1:p.Leu250Gln
NM_000349.3:c.843T>A MANE Select NP_000340.2:p.Ser281=