Canonical Allele Identifier: CA399702448
Gene: SOST HGNC NCBI

Linked Data

gnomAD v4: 17-43755725-G-C
MyVariant Identifiers: chr17:g.41833093G>C (hg19) chr17:g.43755725G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755725G>C , CM000679.2:g.43755725G>C GRCh38
NC_000017.10:g.41833093G>C , CM000679.1:g.41833093G>C GRCh37
NC_000017.9:g.39188619G>C NCBI36
NG_008078.2:g.8064C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.259C>G MANE Select ENSP00000301691.1:p.Arg87Gly
ENST00000301691.2:c.259C>G ENSP00000301691.1:p.Arg87Gly
NM_025237.2:c.259C>G NP_079513.1:p.Arg87Gly
NM_025237.3:c.259C>G MANE Select NP_079513.1:p.Arg87Gly
Search 100 bp 5'
Search 100 bp 3'