Canonical Allele Identifier: CA8592829
Gene: SOST HGNC NCBI

Linked Data

dbSNP Id: rs767409909
ExAC: 17:41833154 G / C
gnomAD v2: 17-41833154-G-C
gnomAD v3: 17-43755786-G-C
gnomAD v4: 17-43755786-G-C
MyVariant Identifiers: chr17:g.41833154G>C (hg19) chr17:g.43755786G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755786G>C , CM000679.2:g.43755786G>C GRCh38
NC_000017.10:g.41833154G>C , CM000679.1:g.41833154G>C GRCh37
NC_000017.9:g.39188680G>C NCBI36
NG_008078.2:g.8003C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.221-23C>G MANE Select ENSP00000301691.1:n.221-23C>G
ENST00000301691.2:c.221-23C>G ENSP00000301691.1:n.221-23C>G
NM_025237.2:c.221-23C>G NP_079513.1:n.221-23C>G
NM_025237.3:c.221-23C>G MANE Select NP_079513.1:n.221-23C>G
Search 100 bp 5'
Search 100 bp 3'