Canonical Allele Identifier: CA370698919
Gene: STAR HGNC NCBI

Linked Data

gnomAD v4: 8-38146002-G-C
MyVariant Identifiers: chr8:g.38003520G>C (hg19) chr8:g.38146002G>C (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000276449.9:c.611C>G MANE Select ENSP00000276449.3:p.Thr204Arg
ENST00000276449.8:c.611C>G ENSP00000276449.3:p.Thr204Arg
ENST00000520114.1:n.1098C>G
ENST00000522050.1:c.547C>G
NM_000349.2:c.611C>G NP_000340.2:p.Thr204Arg
XM_006716392.1:c.611C>G XP_006716455.1:p.Thr204Arg
NM_000349.3:c.611C>G MANE Select NP_000340.2:p.Thr204Arg
Search 100 bp 5'
Search 100 bp 3'