Canonical Allele Identifier: CA8592830
Gene: SOST HGNC NCBI

Linked Data

dbSNP Id: rs749923821
ExAC: 17:41833161 C / G
gnomAD v2: 17-41833161-C-G
gnomAD v3: 17-43755793-C-G
gnomAD v4: 17-43755793-C-G
MyVariant Identifiers: chr17:g.41833161C>G (hg19) chr17:g.43755793C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755793C>G , CM000679.2:g.43755793C>G GRCh38
NC_000017.10:g.41833161C>G , CM000679.1:g.41833161C>G GRCh37
NC_000017.9:g.39188687C>G NCBI36
NG_008078.2:g.7996G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.221-30G>C MANE Select ENSP00000301691.1:n.221-30G>C
ENST00000301691.2:c.221-30G>C ENSP00000301691.1:n.221-30G>C
NM_025237.2:c.221-30G>C NP_079513.1:n.221-30G>C
NM_025237.3:c.221-30G>C MANE Select NP_079513.1:n.221-30G>C
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