Canonical Allele Identifier: CA2261069332
Gene: SOST HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755801T= , CM000679.2:g.43755801T= GRCh38
NC_000017.10:g.41833169T= , CM000679.1:g.41833169T= GRCh37
NC_000017.9:g.39188695T= NCBI36
NG_008078.2:g.7988A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.221-38A= MANE Select ENSP00000301691.1:n.221-38A=
ENST00000301691.2:c.221-38A= ENSP00000301691.1:n.221-38A=
NM_025237.2:c.221-38A= NP_079513.1:n.221-38A=
NM_025237.3:c.221-38A= MANE Select NP_079513.1:n.221-38A=
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