Canonical Allele Identifier: CA290857259
Gene: SOST HGNC NCBI

Linked Data

dbSNP Id: rs933738824
gnomAD v3: 17-43755800-CT-C
gnomAD v4: 17-43755800-CT-C
MyVariant Identifiers: chr17:g.41833169del (hg19) chr17:g.43755801del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755801del , CM000679.2:g.43755801del GRCh38
NC_000017.10:g.41833169del , CM000679.1:g.41833169del GRCh37
NC_000017.9:g.39188695del NCBI36
NG_008078.2:g.7988del

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.221-38del MANE Select ENSP00000301691.1:n.221-38del
ENST00000301691.2:c.221-38del ENSP00000301691.1:n.221-38del
NM_025237.2:c.221-38del NP_079513.1:n.221-38del
NM_025237.3:c.221-38del MANE Select NP_079513.1:n.221-38del
Search 100 bp 5'
Search 100 bp 3'