Canonical Allele Identifier: CA175095561

Gene: STAR

Linked Data

• dbSNP Id: rs140303418
• gnomAD v2: 8-38003130-A-G
• gnomAD v3: 8-38145612-A-G
• gnomAD v4: 8-38145612-A-G
• MyVariant Identifiers: chr8:g.38003130A>G (hg19) ; chr8:g.38145612A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.38145612A>G , CM000670.2:g.38145612A>G	GRCh38
NC_000008.10:g.38003130A>G , CM000670.1:g.38003130A>G	GRCh37
NC_000008.9:g.38122287A>G	NCBI36
NG_011827.1:g.10471T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276449.9:c.651-297T>C MANE Select	ENSP00000276449.3:n.651-297T>C
ENST00000276449.8:c.651-297T>C	ENSP00000276449.3:n.651-297T>C
ENST00000520114.1:n.1488T>C
ENST00000522050.1:c.586+351T>C
NM_000349.2:c.651-297T>C	NP_000340.2:n.651-297T>C
XM_006716392.1:c.650+351T>C	XP_006716455.1:n.650+351T>C
NM_000349.3:c.651-297T>C MANE Select	NP_000340.2:n.651-297T>C