Canonical Allele Identifier: CA460374986
Gene: STAR HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.38002749G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.38145231G>T , CM000670.2:g.38145231G>T GRCh38
NC_000008.10:g.38002749G>T , CM000670.1:g.38002749G>T GRCh37
NC_000008.9:g.38121906G>T NCBI36
NG_011827.1:g.10852C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000276449.9:c.735C>A MANE Select ENSP00000276449.3:p.Ile245=
ENST00000276449.8:c.735C>A ENSP00000276449.3:p.Ile245=
ENST00000520114.1:n.1869C>A
ENST00000522050.1:c.586+732C>A
NM_000349.2:c.735C>A NP_000340.2:p.Ile245=
XM_006716392.1:c.650+732C>A XP_006716455.1:n.650+732C>A
NM_000349.3:c.735C>A MANE Select NP_000340.2:p.Ile245=
Search 100 bp 5'
Search 100 bp 3'