Canonical Allele Identifier: CA626222056
Gene: SOST HGNC NCBI

Linked Data

dbSNP Id: rs1391120831
gnomAD v2: 17-41833150-G-GT
MyVariant Identifiers: chr17:g.41833150_41833151insT (hg19) chr17:g.43755782_43755783insT (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755783dup , CM000679.2:g.43755783dup GRCh38
NC_000017.10:g.41833151dup , CM000679.1:g.41833151dup GRCh37
NC_000017.9:g.39188677dup NCBI36
NG_008078.2:g.8006dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.221-20dup MANE Select ENSP00000301691.1:n.221-20dup
ENST00000301691.2:c.221-20dup ENSP00000301691.1:n.221-20dup
NM_025237.2:c.221-20dup NP_079513.1:n.221-20dup
NM_025237.3:c.221-20dup MANE Select NP_079513.1:n.221-20dup
Search 100 bp 5'
Search 100 bp 3'