Canonical Allele Identifier: CA2261069354
Gene: SOST HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755830T= , CM000679.2:g.43755830T= GRCh38
NC_000017.10:g.41833198T= , CM000679.1:g.41833198T= GRCh37
NC_000017.9:g.39188724T= NCBI36
NG_008078.2:g.7959A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.221-67A= MANE Select ENSP00000301691.1:n.221-67A=
ENST00000301691.2:c.221-67A= ENSP00000301691.1:n.221-67A=
NM_025237.2:c.221-67A= NP_079513.1:n.221-67A=
NM_025237.3:c.221-67A= MANE Select NP_079513.1:n.221-67A=
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