Canonical Allele Identifier: CA772231007
Gene: SOST HGNC NCBI

Linked Data

dbSNP Id: rs1420439890
gnomAD v3: 17-43755822-G-A
gnomAD v4: 17-43755822-G-A
MyVariant Identifiers: chr17:g.41833190G>A (hg19) chr17:g.43755822G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755822G>A , CM000679.2:g.43755822G>A GRCh38
NC_000017.10:g.41833190G>A , CM000679.1:g.41833190G>A GRCh37
NC_000017.9:g.39188716G>A NCBI36
NG_008078.2:g.7967C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.221-59C>T MANE Select ENSP00000301691.1:n.221-59C>T
ENST00000301691.2:c.221-59C>T ENSP00000301691.1:n.221-59C>T
NM_025237.2:c.221-59C>T NP_079513.1:n.221-59C>T
NM_025237.3:c.221-59C>T MANE Select NP_079513.1:n.221-59C>T
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