Canonical Allele Identifier: CA399701165
Gene: SOST HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.41832726A>G (hg19) chr17:g.43755358A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755358A>G , CM000679.2:g.43755358A>G GRCh38
NC_000017.10:g.41832726A>G , CM000679.1:g.41832726A>G GRCh37
NC_000017.9:g.39188252A>G NCBI36
NG_008078.2:g.8431T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.626T>C MANE Select ENSP00000301691.1:p.Leu209Pro
ENST00000301691.2:c.626T>C ENSP00000301691.1:p.Leu209Pro
NM_025237.2:c.626T>C NP_079513.1:p.Leu209Pro
NM_025237.3:c.626T>C MANE Select NP_079513.1:p.Leu209Pro
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Search 100 bp 3'