Canonical Allele Identifier: CA290856861
Gene: SOST HGNC NCBI

Linked Data

dbSNP Id: rs774883248
gnomAD v3: 17-43755387-G-A
gnomAD v4: 17-43755387-G-A
MyVariant Identifiers: chr17:g.41832755G>A (hg19) chr17:g.43755387G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755387G>A , CM000679.2:g.43755387G>A GRCh38
NC_000017.10:g.41832755G>A , CM000679.1:g.41832755G>A GRCh37
NC_000017.9:g.39188281G>A NCBI36
NG_008078.2:g.8402C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.597C>T MANE Select ENSP00000301691.1:p.Ala199=
ENST00000301691.2:c.597C>T ENSP00000301691.1:p.Ala199=
NM_025237.2:c.597C>T NP_079513.1:p.Ala199=
NM_025237.3:c.597C>T MANE Select NP_079513.1:p.Ala199=
Search 100 bp 5'
Search 100 bp 3'