Canonical Allele Identifier: CA399702578
Gene: SOST HGNC NCBI

Linked Data

dbSNP Id: rs1405992033
MyVariant Identifiers: chr17:g.41833128A>C (hg19) chr17:g.43755760A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755760A>C , CM000679.2:g.43755760A>C GRCh38
NC_000017.10:g.41833128A>C , CM000679.1:g.41833128A>C GRCh37
NC_000017.9:g.39188654A>C NCBI36
NG_008078.2:g.8029T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.224T>G MANE Select ENSP00000301691.1:p.Val75Gly
ENST00000301691.2:c.224T>G ENSP00000301691.1:p.Val75Gly
NM_025237.2:c.224T>G NP_079513.1:p.Val75Gly
NM_025237.3:c.224T>G MANE Select NP_079513.1:p.Val75Gly
Search 100 bp 5'
Search 100 bp 3'