Canonical Allele Identifier: CA2261069345
Gene: SOST HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755814C= , CM000679.2:g.43755814C= GRCh38
NC_000017.10:g.41833182C= , CM000679.1:g.41833182C= GRCh37
NC_000017.9:g.39188708C= NCBI36
NG_008078.2:g.7975G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.221-51G= MANE Select ENSP00000301691.1:n.221-51G=
ENST00000301691.2:c.221-51G= ENSP00000301691.1:n.221-51G=
NM_025237.2:c.221-51G= NP_079513.1:n.221-51G=
NM_025237.3:c.221-51G= MANE Select NP_079513.1:n.221-51G=
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