Canonical Allele Identifier: CA2261069342
Gene: SOST HGNC NCBI

Linked Data

dbSNP Id: rs567348306
gnomAD v4: 17-43755811-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755811T>C , CM000679.2:g.43755811T>C GRCh38
NC_000017.10:g.41833179T>C , CM000679.1:g.41833179T>C GRCh37
NC_000017.9:g.39188705T>C NCBI36
NG_008078.2:g.7978A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.221-48A>G MANE Select ENSP00000301691.1:n.221-48A>G
ENST00000301691.2:c.221-48A>G ENSP00000301691.1:n.221-48A>G
NM_025237.2:c.221-48A>G NP_079513.1:n.221-48A>G
NM_025237.3:c.221-48A>G MANE Select NP_079513.1:n.221-48A>G
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