Canonical Allele Identifier: CA370698921
Gene: STAR HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.38003520G>T (hg19) chr8:g.38146002G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.38146002G>T , CM000670.2:g.38146002G>T GRCh38
NC_000008.10:g.38003520G>T , CM000670.1:g.38003520G>T GRCh37
NC_000008.9:g.38122677G>T NCBI36
NG_011827.1:g.10081C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000276449.9:c.611C>A MANE Select ENSP00000276449.3:p.Thr204Lys
ENST00000276449.8:c.611C>A ENSP00000276449.3:p.Thr204Lys
ENST00000520114.1:n.1098C>A
ENST00000522050.1:c.547C>A
NM_000349.2:c.611C>A NP_000340.2:p.Thr204Lys
XM_006716392.1:c.611C>A XP_006716455.1:p.Thr204Lys
NM_000349.3:c.611C>A MANE Select NP_000340.2:p.Thr204Lys
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