Canonical Allele Identifier: CA399701435
Gene: SOST HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.41832807A>T (hg19) chr17:g.43755439A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755439A>T , CM000679.2:g.43755439A>T GRCh38
NC_000017.10:g.41832807A>T , CM000679.1:g.41832807A>T GRCh37
NC_000017.9:g.39188333A>T NCBI36
NG_008078.2:g.8350T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.545T>A MANE Select ENSP00000301691.1:p.Phe182Tyr
ENST00000301691.2:c.545T>A ENSP00000301691.1:p.Phe182Tyr
NM_025237.2:c.545T>A NP_079513.1:p.Phe182Tyr
NM_025237.3:c.545T>A MANE Select NP_079513.1:p.Phe182Tyr
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