Canonical Allele Identifier: CA399702100
Gene: SOST HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.41833002T>A (hg19) chr17:g.43755634T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755634T>A , CM000679.2:g.43755634T>A GRCh38
NC_000017.10:g.41833002T>A , CM000679.1:g.41833002T>A GRCh37
NC_000017.9:g.39188528T>A NCBI36
NG_008078.2:g.8155A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.350A>T MANE Select ENSP00000301691.1:p.Asn117Ile
ENST00000301691.2:c.350A>T ENSP00000301691.1:p.Asn117Ile
NM_025237.2:c.350A>T NP_079513.1:p.Asn117Ile
NM_025237.3:c.350A>T MANE Select NP_079513.1:p.Asn117Ile
Search 100 bp 5'
Search 100 bp 3'