Canonical Allele Identifier: CA460497017
Gene: STAR HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.38003654C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.38146136C>T , CM000670.2:g.38146136C>T GRCh38
NC_000008.10:g.38003654C>T , CM000670.1:g.38003654C>T GRCh37
NC_000008.9:g.38122811C>T NCBI36
NG_011827.1:g.9947G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000276449.9:c.477G>A MANE Select ENSP00000276449.3:p.Lys159=
ENST00000276449.8:c.477G>A ENSP00000276449.3:p.Lys159=
ENST00000520114.1:n.964G>A
ENST00000522050.1:c.413G>A
NM_000349.2:c.477G>A NP_000340.2:p.Lys159=
XM_006716392.1:c.477G>A XP_006716455.1:p.Lys159=
NM_000349.3:c.477G>A MANE Select NP_000340.2:p.Lys159=
Search 100 bp 5'
Search 100 bp 3'