Canonical Allele Identifier: CA2638110328
Gene: SOST HGNC NCBI

Linked Data

gnomAD v4: 17-43755849-CT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755853del , CM000679.2:g.43755853del GRCh38
NC_000017.10:g.41833221del , CM000679.1:g.41833221del GRCh37
NC_000017.9:g.39188747del NCBI36
NG_008078.2:g.7939del

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.221-87del MANE Select ENSP00000301691.1:n.221-87del
ENST00000301691.2:c.221-87del ENSP00000301691.1:n.221-87del
NM_025237.2:c.221-87del NP_079513.1:n.221-87del
NM_025237.3:c.221-87del MANE Select NP_079513.1:n.221-87del
Search 100 bp 5'
Search 100 bp 3'