Canonical Allele Identifier: CA2261069322
Gene: SOST HGNC NCBI

Linked Data

dbSNP Id: rs1598296196
gnomAD v4: 17-43755789-T-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755789T>G , CM000679.2:g.43755789T>G GRCh38
NC_000017.10:g.41833157T>G , CM000679.1:g.41833157T>G GRCh37
NC_000017.9:g.39188683T>G NCBI36
NG_008078.2:g.8000A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.221-26A>C MANE Select ENSP00000301691.1:n.221-26A>C
ENST00000301691.2:c.221-26A>C ENSP00000301691.1:n.221-26A>C
NM_025237.2:c.221-26A>C NP_079513.1:n.221-26A>C
NM_025237.3:c.221-26A>C MANE Select NP_079513.1:n.221-26A>C
Search 100 bp 5'
Search 100 bp 3'