Canonical Allele Identifier: CA2261069326
Gene: SOST HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755794G= , CM000679.2:g.43755794G= GRCh38
NC_000017.10:g.41833162G= , CM000679.1:g.41833162G= GRCh37
NC_000017.9:g.39188688G= NCBI36
NG_008078.2:g.7995C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.221-31C= MANE Select ENSP00000301691.1:n.221-31C=
ENST00000301691.2:c.221-31C= ENSP00000301691.1:n.221-31C=
NM_025237.2:c.221-31C= NP_079513.1:n.221-31C=
NM_025237.3:c.221-31C= MANE Select NP_079513.1:n.221-31C=
Search 100 bp 5'
Search 100 bp 3'