Canonical Allele Identifier: CA399702466
Gene: SOST HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.41833098A>C (hg19) chr17:g.43755730A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755730A>C , CM000679.2:g.43755730A>C GRCh38
NC_000017.10:g.41833098A>C , CM000679.1:g.41833098A>C GRCh37
NC_000017.9:g.39188624A>C NCBI36
NG_008078.2:g.8059T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.254T>G MANE Select ENSP00000301691.1:p.Phe85Cys
ENST00000301691.2:c.254T>G ENSP00000301691.1:p.Phe85Cys
NM_025237.2:c.254T>G NP_079513.1:p.Phe85Cys
NM_025237.3:c.254T>G MANE Select NP_079513.1:p.Phe85Cys
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