Canonical Allele Identifier: CA626222061
Gene: SOST HGNC NCBI

Linked Data

dbSNP Id: rs1159438668
gnomAD v2: 17-41833180-GC-G
gnomAD v4: 17-43755812-GC-G
MyVariant Identifiers: chr17:g.41833181del (hg19) chr17:g.43755813del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755815del , CM000679.2:g.43755815del GRCh38
NC_000017.10:g.41833183del , CM000679.1:g.41833183del GRCh37
NC_000017.9:g.39188709del NCBI36
NG_008078.2:g.7976del

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.221-50del MANE Select ENSP00000301691.1:n.221-50del
ENST00000301691.2:c.221-50del ENSP00000301691.1:n.221-50del
NM_025237.2:c.221-50del NP_079513.1:n.221-50del
NM_025237.3:c.221-50del MANE Select NP_079513.1:n.221-50del
Search 100 bp 5'
Search 100 bp 3'