Canonical Allele Identifier: CA2638110342
Gene: SOST HGNC NCBI

Linked Data

gnomAD v4: 17-43755862-T-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755862T>A , CM000679.2:g.43755862T>A GRCh38
NC_000017.10:g.41833230T>A , CM000679.1:g.41833230T>A GRCh37
NC_000017.9:g.39188756T>A NCBI36
NG_008078.2:g.7927A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.221-99A>T MANE Select ENSP00000301691.1:n.221-99A>T
ENST00000301691.2:c.221-99A>T ENSP00000301691.1:n.221-99A>T
NM_025237.2:c.221-99A>T NP_079513.1:n.221-99A>T
NM_025237.3:c.221-99A>T MANE Select NP_079513.1:n.221-99A>T
Search 100 bp 5'
Search 100 bp 3'