Canonical Allele Identifier: CA2261069241
Gene: SOST HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755627G= , CM000679.2:g.43755627G= GRCh38
NC_000017.10:g.41832995G= , CM000679.1:g.41832995G= GRCh37
NC_000017.9:g.39188521G= NCBI36
NG_008078.2:g.8162C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.357C= MANE Select ENSP00000301691.1:p.Ile119=
ENST00000301691.2:c.357C= ENSP00000301691.1:p.Ile119=
NM_025237.2:c.357C= NP_079513.1:p.Ile119=
NM_025237.3:c.357C= MANE Select NP_079513.1:p.Ile119=