Canonical Allele Identifier: CA1777410488
Gene: STAR HGNC NCBI

Linked Data

dbSNP Id: rs1563267666

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.38145581T>C , CM000670.2:g.38145581T>C GRCh38
NC_000008.10:g.38003099T>C , CM000670.1:g.38003099T>C GRCh37
NC_000008.9:g.38122256T>C NCBI36
NG_011827.1:g.10502A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000276449.9:c.651-266A>G MANE Select ENSP00000276449.3:n.651-266A>G
ENST00000276449.8:c.651-266A>G ENSP00000276449.3:n.651-266A>G
ENST00000520114.1:n.1519A>G
ENST00000522050.1:c.586+382A>G
NM_000349.2:c.651-266A>G NP_000340.2:n.651-266A>G
XM_006716392.1:c.650+382A>G XP_006716455.1:n.650+382A>G
NM_000349.3:c.651-266A>G MANE Select NP_000340.2:n.651-266A>G