Canonical Allele Identifier: CA2638110313
Gene: SOST HGNC NCBI

Linked Data

gnomAD v4: 17-43755834-T-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755834T>C , CM000679.2:g.43755834T>C GRCh38
NC_000017.10:g.41833202T>C , CM000679.1:g.41833202T>C GRCh37
NC_000017.9:g.39188728T>C NCBI36
NG_008078.2:g.7955A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.221-71A>G MANE Select ENSP00000301691.1:n.221-71A>G
ENST00000301691.2:c.221-71A>G ENSP00000301691.1:n.221-71A>G
NM_025237.2:c.221-71A>G NP_079513.1:n.221-71A>G
NM_025237.3:c.221-71A>G MANE Select NP_079513.1:n.221-71A>G
Search 100 bp 5'
Search 100 bp 3'