Canonical Allele Identifier: CA399702232
Gene: SOST HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.41833038C>T (hg19) chr17:g.43755670C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755670C>T , CM000679.2:g.43755670C>T GRCh38
NC_000017.10:g.41833038C>T , CM000679.1:g.41833038C>T GRCh37
NC_000017.9:g.39188564C>T NCBI36
NG_008078.2:g.8119G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.314G>A MANE Select ENSP00000301691.1:p.Cys105Tyr
ENST00000301691.2:c.314G>A ENSP00000301691.1:p.Cys105Tyr
NM_025237.2:c.314G>A NP_079513.1:p.Cys105Tyr
NM_025237.3:c.314G>A MANE Select NP_079513.1:p.Cys105Tyr
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