Canonical Allele Identifier: CA370696799
Gene: STAR HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.38002763A>C (hg19) chr8:g.38145245A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.38145245A>C , CM000670.2:g.38145245A>C GRCh38
NC_000008.10:g.38002763A>C , CM000670.1:g.38002763A>C GRCh37
NC_000008.9:g.38121920A>C NCBI36
NG_011827.1:g.10838T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000276449.9:c.721T>G MANE Select ENSP00000276449.3:p.Trp241Gly
ENST00000276449.8:c.721T>G ENSP00000276449.3:p.Trp241Gly
ENST00000520114.1:n.1855T>G
ENST00000522050.1:c.586+718T>G
NM_000349.2:c.721T>G NP_000340.2:p.Trp241Gly
XM_006716392.1:c.650+718T>G XP_006716455.1:n.650+718T>G
NM_000349.3:c.721T>G MANE Select NP_000340.2:p.Trp241Gly
Search 100 bp 5'
Search 100 bp 3'