Canonical Allele Identifier: CA626222058
Gene: SOST HGNC NCBI

Linked Data

dbSNP Id: rs1386030834
gnomAD v2: 17-41833153-AGGGTGGCCGCCCGCCT-A
gnomAD v4: 17-43755785-AGGGTGGCCGCCCGCCT-A
MyVariant Identifiers: chr17:g.41833154_41833169del (hg19) chr17:g.43755786_43755801del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755788_43755803del , CM000679.2:g.43755788_43755803del GRCh38
NC_000017.10:g.41833156_41833171del , CM000679.1:g.41833156_41833171del GRCh37
NC_000017.9:g.39188682_39188697del NCBI36
NG_008078.2:g.7988_8003del

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.221-38_221-23del MANE Select ENSP00000301691.1:n.221-38_221-23del
ENST00000301691.2:c.221-38_221-23del ENSP00000301691.1:n.221-38_221-23del
NM_025237.2:c.221-38_221-23del NP_079513.1:n.221-38_221-23del
NM_025237.3:c.221-38_221-23del MANE Select NP_079513.1:n.221-38_221-23del
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