Canonical Allele Identifier: CA2686932735
Gene: STAR HGNC NCBI

Linked Data

gnomAD v4: 8-38145818-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.38145818A>T , CM000670.2:g.38145818A>T GRCh38
NC_000008.10:g.38003336A>T , CM000670.1:g.38003336A>T GRCh37
NC_000008.9:g.38122493A>T NCBI36
NG_011827.1:g.10265T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000276449.9:c.650+145T>A MANE Select ENSP00000276449.3:n.650+145T>A
ENST00000276449.8:c.650+145T>A ENSP00000276449.3:n.650+145T>A
ENST00000520114.1:n.1282T>A
ENST00000522050.1:c.586+145T>A
NM_000349.2:c.650+145T>A NP_000340.2:n.650+145T>A
XM_006716392.1:c.650+145T>A XP_006716455.1:n.650+145T>A
NM_000349.3:c.650+145T>A MANE Select NP_000340.2:n.650+145T>A