Canonical Allele Identifier: CA175091189
Gene: STAR HGNC NCBI
ClinVar Variation:
gnomAD v4:
MyVariant.info:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.38144387C>G , CM000670.2:g.38144387C>G GRCh38
NC_000008.10:g.38001905C>G , CM000670.1:g.38001905C>G GRCh37
NC_000008.9:g.38121062C>G NCBI36
NG_011827.1:g.11696G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000276449.9:c.745-1G>C MANE Select ENSP00000276449.3:n.745-1G>C
ENST00000276449.8:c.745-1G>C ENSP00000276449.3:n.745-1G>C
ENST00000520114.1:n.2713G>C
ENST00000522050.1:c.587-1G>C
NM_000349.2:c.745-1G>C NP_000340.2:n.745-1G>C
XM_006716392.1:c.651-1G>C XP_006716455.1:n.651-1G>C
NM_000349.3:c.745-1G>C MANE Select NP_000340.2:n.745-1G>C