Canonical Allele Identifier: CA2261069327
Gene: SOST HGNC NCBI

Linked Data

dbSNP Id: rs760140099
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755794G>C , CM000679.2:g.43755794G>C GRCh38
NC_000017.10:g.41833162G>C , CM000679.1:g.41833162G>C GRCh37
NC_000017.9:g.39188688G>C NCBI36
NG_008078.2:g.7995C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.221-31C>G MANE Select ENSP00000301691.1:n.221-31C>G
ENST00000301691.2:c.221-31C>G ENSP00000301691.1:n.221-31C>G
NM_025237.2:c.221-31C>G NP_079513.1:n.221-31C>G
NM_025237.3:c.221-31C>G MANE Select NP_079513.1:n.221-31C>G
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