Canonical Allele Identifier: CA983938005
Gene: SOST HGNC NCBI

Linked Data

dbSNP Id: rs1974125326
gnomAD v3: 17-43755827-G-GTC
gnomAD v4: 17-43755827-G-GTC
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755834_43755835dup , CM000679.2:g.43755834_43755835dup GRCh38
NC_000017.10:g.41833202_41833203dup , CM000679.1:g.41833202_41833203dup GRCh37
NC_000017.9:g.39188728_39188729dup NCBI36
NG_008078.2:g.7960_7961dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.221-66_221-65dup MANE Select ENSP00000301691.1:n.221-66_221-65dup
ENST00000301691.2:c.221-66_221-65dup ENSP00000301691.1:n.221-66_221-65dup
NM_025237.2:c.221-66_221-65dup NP_079513.1:n.221-66_221-65dup
NM_025237.3:c.221-66_221-65dup MANE Select NP_079513.1:n.221-66_221-65dup
Search 100 bp 5'
Search 100 bp 3'