Canonical Allele Identifier: CA399701645
Gene: SOST HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755497C>A , CM000679.2:g.43755497C>A GRCh38
NC_000017.10:g.41832865C>A , CM000679.1:g.41832865C>A GRCh37
NC_000017.9:g.39188391C>A NCBI36
NG_008078.2:g.8292G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.487G>T MANE Select ENSP00000301691.1:p.Ala163Ser
ENST00000301691.2:c.487G>T ENSP00000301691.1:p.Ala163Ser
NM_025237.2:c.487G>T NP_079513.1:p.Ala163Ser
NM_025237.3:c.487G>T MANE Select NP_079513.1:p.Ala163Ser