Canonical Allele Identifier: CA626094806
Gene: SOST HGNC NCBI

Linked Data

dbSNP Id: rs1205766295
gnomAD v2: 17-41832702-G-C
gnomAD v4: 17-43755334-G-C
MyVariant Identifiers: chr17:g.41832702G>C (hg19) chr17:g.43755334G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755334G>C , CM000679.2:g.43755334G>C GRCh38
NC_000017.10:g.41832702G>C , CM000679.1:g.41832702G>C GRCh37
NC_000017.9:g.39188228G>C NCBI36
NG_008078.2:g.8455C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.*8C>G MANE Select ENSP00000301691.1:n.*8C>G
ENST00000301691.2:c.*8C>G ENSP00000301691.1:n.*8C>G
NM_025237.2:c.*8C>G NP_079513.1:n.*8C>G
NM_025237.3:c.*8C>G MANE Select NP_079513.1:n.*8C>G
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