Canonical Allele Identifier: CA851447449

Gene: STAR

Linked Data

• dbSNP Id: rs1453730730
• gnomAD v3: 8-38145875-G-C
• gnomAD v4: 8-38145875-G-C
• MyVariant Identifiers: chr8:g.38003393G>C (hg19) ; chr8:g.38145875G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.38145875G>C , CM000670.2:g.38145875G>C	GRCh38
NC_000008.10:g.38003393G>C , CM000670.1:g.38003393G>C	GRCh37
NC_000008.9:g.38122550G>C	NCBI36
NG_011827.1:g.10208C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000276449.9:c.650+88C>G MANE Select	ENSP00000276449.3:n.650+88C>G
ENST00000276449.8:c.650+88C>G	ENSP00000276449.3:n.650+88C>G
ENST00000520114.1:n.1225C>G
ENST00000522050.1:c.586+88C>G
NM_000349.2:c.650+88C>G	NP_000340.2:n.650+88C>G
XM_006716392.1:c.650+88C>G	XP_006716455.1:n.650+88C>G
NM_000349.3:c.650+88C>G MANE Select	NP_000340.2:n.650+88C>G