Canonical Allele Identifier: CA8592832
Gene: SOST HGNC NCBI

Linked Data

dbSNP Id: rs766016242
ExAC: 17:41833165 C / T
gnomAD v2: 17-41833165-C-T
gnomAD v3: 17-43755797-C-T
gnomAD v4: 17-43755797-C-T
MyVariant Identifiers: chr17:g.41833165C>T (hg19) chr17:g.43755797C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755797C>T , CM000679.2:g.43755797C>T GRCh38
NC_000017.10:g.41833165C>T , CM000679.1:g.41833165C>T GRCh37
NC_000017.9:g.39188691C>T NCBI36
NG_008078.2:g.7992G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.221-34G>A MANE Select ENSP00000301691.1:n.221-34G>A
ENST00000301691.2:c.221-34G>A ENSP00000301691.1:n.221-34G>A
NM_025237.2:c.221-34G>A NP_079513.1:n.221-34G>A
NM_025237.3:c.221-34G>A MANE Select NP_079513.1:n.221-34G>A
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