Canonical Allele Identifier: CA2638110293
Gene: SOST HGNC NCBI

Linked Data

gnomAD v4: 17-43755816-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755816T>G , CM000679.2:g.43755816T>G GRCh38
NC_000017.10:g.41833184T>G , CM000679.1:g.41833184T>G GRCh37
NC_000017.9:g.39188710T>G NCBI36
NG_008078.2:g.7973A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.221-53A>C MANE Select ENSP00000301691.1:n.221-53A>C
ENST00000301691.2:c.221-53A>C ENSP00000301691.1:n.221-53A>C
NM_025237.2:c.221-53A>C NP_079513.1:n.221-53A>C
NM_025237.3:c.221-53A>C MANE Select NP_079513.1:n.221-53A>C
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