Canonical Allele Identifier: CA2261069140
Gene: SOST HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755419G= , CM000679.2:g.43755419G= GRCh38
NC_000017.10:g.41832787G= , CM000679.1:g.41832787G= GRCh37
NC_000017.9:g.39188313G= NCBI36
NG_008078.2:g.8370C=

Transcript Alleles

HGVS Amino-acid change
ENST00000301691.3:c.565C= MANE Select ENSP00000301691.1:p.Pro189=
ENST00000301691.2:c.565C= ENSP00000301691.1:p.Pro189=
NM_025237.2:c.565C= NP_079513.1:p.Pro189=
NM_025237.3:c.565C= MANE Select NP_079513.1:p.Pro189=