Canonical Allele Identifier: CA370695466
Gene: STAR HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.38001794A>C (hg19) chr8:g.38144276A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.38144276A>C , CM000670.2:g.38144276A>C GRCh38
NC_000008.10:g.38001794A>C , CM000670.1:g.38001794A>C GRCh37
NC_000008.9:g.38120951A>C NCBI36
NG_011827.1:g.11807T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000276449.9:c.855T>G MANE Select ENSP00000276449.3:p.Cys285Trp
ENST00000276449.8:c.855T>G ENSP00000276449.3:p.Cys285Trp
ENST00000520114.1:n.2824T>G
ENST00000522050.1:c.697T>G
NM_000349.2:c.855T>G NP_000340.2:p.Cys285Trp
XM_006716392.1:c.761T>G XP_006716455.1:p.Val254Gly
NM_000349.3:c.855T>G MANE Select NP_000340.2:p.Cys285Trp
Search 100 bp 5'
Search 100 bp 3'