Canonical Allele Identifier: CA500234859
Gene: SOST HGNC NCBI

Linked Data

gnomAD v4: 17-43755408-G-C
MyVariant Identifiers: chr17:g.41832776G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755408G>C , CM000679.2:g.43755408G>C GRCh38
NC_000017.10:g.41832776G>C , CM000679.1:g.41832776G>C GRCh37
NC_000017.9:g.39188302G>C NCBI36
NG_008078.2:g.8381C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.576C>G MANE Select ENSP00000301691.1:p.Gly192=
ENST00000301691.2:c.576C>G ENSP00000301691.1:p.Gly192=
NM_025237.2:c.576C>G NP_079513.1:p.Gly192=
NM_025237.3:c.576C>G MANE Select NP_079513.1:p.Gly192=
Search 100 bp 5'
Search 100 bp 3'