Canonical Allele Identifier: CA2261069341
Gene: SOST HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755811T= , CM000679.2:g.43755811T= GRCh38
NC_000017.10:g.41833179T= , CM000679.1:g.41833179T= GRCh37
NC_000017.9:g.39188705T= NCBI36
NG_008078.2:g.7978A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.221-48A= MANE Select ENSP00000301691.1:n.221-48A=
ENST00000301691.2:c.221-48A= ENSP00000301691.1:n.221-48A=
NM_025237.2:c.221-48A= NP_079513.1:n.221-48A=
NM_025237.3:c.221-48A= MANE Select NP_079513.1:n.221-48A=
Search 100 bp 5'
Search 100 bp 3'