Canonical Allele Identifier: CA399701797
Gene: SOST HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755547A>T , CM000679.2:g.43755547A>T GRCh38
NC_000017.10:g.41832915A>T , CM000679.1:g.41832915A>T GRCh37
NC_000017.9:g.39188441A>T NCBI36
NG_008078.2:g.8242T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.437T>A MANE Select ENSP00000301691.1:p.Leu146Gln
ENST00000301691.2:c.437T>A ENSP00000301691.1:p.Leu146Gln
NM_025237.2:c.437T>A NP_079513.1:p.Leu146Gln
NM_025237.3:c.437T>A MANE Select NP_079513.1:p.Leu146Gln