Canonical Allele Identifier: CA175091720
Gene: STAR HGNC NCBI

Linked Data

dbSNP Id: rs982982152
gnomAD v4: 8-38145142-T-A
MyVariant Identifiers: chr8:g.38145142T>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.38145142T>A , CM000670.2:g.38145142T>A GRCh38
NC_000008.10:g.38002660T>A , CM000670.1:g.38002660T>A GRCh37
NC_000008.9:g.38121817T>A NCBI36
NG_011827.1:g.10941A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000276449.9:c.744+80A>T MANE Select ENSP00000276449.3:n.744+80A>T
ENST00000276449.8:c.744+80A>T ENSP00000276449.3:n.744+80A>T
ENST00000520114.1:n.1958A>T
ENST00000522050.1:c.587-756A>T
NM_000349.2:c.744+80A>T NP_000340.2:n.744+80A>T
XM_006716392.1:c.651-756A>T XP_006716455.1:n.651-756A>T
NM_000349.3:c.744+80A>T MANE Select NP_000340.2:n.744+80A>T