Canonical Allele Identifier: CA983937644
Gene: SOST HGNC NCBI

Linked Data

dbSNP Id: rs1814443631
gnomAD v3: 17-43755391-CG-C
gnomAD v4: 17-43755391-CG-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755395del , CM000679.2:g.43755395del GRCh38
NC_000017.10:g.41832763del , CM000679.1:g.41832763del GRCh37
NC_000017.9:g.39188289del NCBI36
NG_008078.2:g.8397del

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.592del MANE Select ENSP00000301691.1:p.Arg198AlafsTer?
ENST00000301691.2:c.592del ENSP00000301691.1:p.Arg198AlafsTer?
NM_025237.2:c.592del NP_079513.1:p.Arg198AlafsTer?
NM_025237.3:c.592del MANE Select NP_079513.1:p.Arg198AlafsTer?
Search 100 bp 5'
Search 100 bp 3'