Canonical Allele Identifier: CA399702272
Gene: SOST HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755682G>T , CM000679.2:g.43755682G>T GRCh38
NC_000017.10:g.41833050G>T , CM000679.1:g.41833050G>T GRCh37
NC_000017.9:g.39188576G>T NCBI36
NG_008078.2:g.8107C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.302C>A MANE Select ENSP00000301691.1:p.Thr101Asn
ENST00000301691.2:c.302C>A ENSP00000301691.1:p.Thr101Asn
NM_025237.2:c.302C>A NP_079513.1:p.Thr101Asn
NM_025237.3:c.302C>A MANE Select NP_079513.1:p.Thr101Asn