Canonical Allele Identifier: CA2261069340
Gene: SOST HGNC NCBI

Linked Data

dbSNP Id: rs778214957
gnomAD v4: 17-43755810-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755810C>T , CM000679.2:g.43755810C>T GRCh38
NC_000017.10:g.41833178C>T , CM000679.1:g.41833178C>T GRCh37
NC_000017.9:g.39188704C>T NCBI36
NG_008078.2:g.7979G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.221-47G>A MANE Select ENSP00000301691.1:n.221-47G>A
ENST00000301691.2:c.221-47G>A ENSP00000301691.1:n.221-47G>A
NM_025237.2:c.221-47G>A NP_079513.1:n.221-47G>A
NM_025237.3:c.221-47G>A MANE Select NP_079513.1:n.221-47G>A
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