Canonical Allele Identifier: CA370698900
Gene: STAR HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.38003515A>C (hg19) chr8:g.38145997A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.38145997A>C , CM000670.2:g.38145997A>C GRCh38
NC_000008.10:g.38003515A>C , CM000670.1:g.38003515A>C GRCh37
NC_000008.9:g.38122672A>C NCBI36
NG_011827.1:g.10086T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000276449.9:c.616T>G MANE Select ENSP00000276449.3:p.Phe206Val
ENST00000276449.8:c.616T>G ENSP00000276449.3:p.Phe206Val
ENST00000520114.1:n.1103T>G
ENST00000522050.1:c.552T>G
NM_000349.2:c.616T>G NP_000340.2:p.Phe206Val
XM_006716392.1:c.616T>G XP_006716455.1:p.Phe206Val
NM_000349.3:c.616T>G MANE Select NP_000340.2:p.Phe206Val
Search 100 bp 5'
Search 100 bp 3'