Canonical Allele Identifier: CA2261069291
Gene: SOST HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755731A= , CM000679.2:g.43755731A= GRCh38
NC_000017.10:g.41833099A= , CM000679.1:g.41833099A= GRCh37
NC_000017.9:g.39188625A= NCBI36
NG_008078.2:g.8058T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.253T= MANE Select ENSP00000301691.1:p.Phe85=
ENST00000301691.2:c.253T= ENSP00000301691.1:p.Phe85=
NM_025237.2:c.253T= NP_079513.1:p.Phe85=
NM_025237.3:c.253T= MANE Select NP_079513.1:p.Phe85=
Search 100 bp 5'
Search 100 bp 3'