Canonical Allele Identifier: CA4715187
Gene: STAR HGNC NCBI

Linked Data

dbSNP Id: rs773048263
gnomAD v2: 8-38003441-T-C
gnomAD v4: 8-38145923-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.38145923T>C , CM000670.2:g.38145923T>C GRCh38
NC_000008.10:g.38003441T>C , CM000670.1:g.38003441T>C GRCh37
NC_000008.9:g.38122598T>C NCBI36
NG_011827.1:g.10160A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000276449.9:c.650+40A>G MANE Select ENSP00000276449.3:n.650+40A>G
ENST00000276449.8:c.650+40A>G ENSP00000276449.3:n.650+40A>G
ENST00000520114.1:n.1177A>G
ENST00000522050.1:c.586+40A>G
NM_000349.2:c.650+40A>G NP_000340.2:n.650+40A>G
XM_006716392.1:c.650+40A>G XP_006716455.1:n.650+40A>G
NM_000349.3:c.650+40A>G MANE Select NP_000340.2:n.650+40A>G