Canonical Allele Identifier: CA1777410688
Gene: STAR HGNC NCBI

Linked Data

dbSNP Id: rs1193299808
gnomAD v4: 8-38145795-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.38145795C>G , CM000670.2:g.38145795C>G GRCh38
NC_000008.10:g.38003313C>G , CM000670.1:g.38003313C>G GRCh37
NC_000008.9:g.38122470C>G NCBI36
NG_011827.1:g.10288G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000276449.9:c.650+168G>C MANE Select ENSP00000276449.3:n.650+168G>C
ENST00000276449.8:c.650+168G>C ENSP00000276449.3:n.650+168G>C
ENST00000520114.1:n.1305G>C
ENST00000522050.1:c.586+168G>C
NM_000349.2:c.650+168G>C NP_000340.2:n.650+168G>C
XM_006716392.1:c.650+168G>C XP_006716455.1:n.650+168G>C
NM_000349.3:c.650+168G>C MANE Select NP_000340.2:n.650+168G>C