Canonical Allele Identifier: CA500235000
Gene: SOST HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.41832902A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755534A>C , CM000679.2:g.43755534A>C GRCh38
NC_000017.10:g.41832902A>C , CM000679.1:g.41832902A>C GRCh37
NC_000017.9:g.39188428A>C NCBI36
NG_008078.2:g.8255T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.450T>G MANE Select ENSP00000301691.1:p.Gly150=
ENST00000301691.2:c.450T>G ENSP00000301691.1:p.Gly150=
NM_025237.2:c.450T>G NP_079513.1:p.Gly150=
NM_025237.3:c.450T>G MANE Select NP_079513.1:p.Gly150=
Search 100 bp 5'
Search 100 bp 3'