Canonical Allele Identifier: CA2261069095
Gene: SOST HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755335G= , CM000679.2:g.43755335G= GRCh38
NC_000017.10:g.41832703G= , CM000679.1:g.41832703G= GRCh37
NC_000017.9:g.39188229G= NCBI36
NG_008078.2:g.8454C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.*7C= MANE Select ENSP00000301691.1:n.*7C=
ENST00000301691.2:c.*7C= ENSP00000301691.1:n.*7C=
NM_025237.2:c.*7C= NP_079513.1:n.*7C=
NM_025237.3:c.*7C= MANE Select NP_079513.1:n.*7C=
Search 100 bp 5'
Search 100 bp 3'