Canonical Allele Identifier: CA2013130361
Gene: FGF23 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4372533C= , CM000674.2:g.4372533C= GRCh38
NC_000012.11:g.4481699C= , CM000674.1:g.4481699C= GRCh37
NC_000012.10:g.4351960C= NCBI36
NG_007087.1:g.12196G=

Transcript Alleles

HGVS Amino-acid change
ENST00000237837.2:c.315+61G= MANE Select ENSP00000237837.1:n.315+61G=
ENST00000648100.1:c.*1967+6251C= ENSP00000497536.1:n.*1967+6251C=
ENST00000648269.1:n.1815+61G=
ENST00000674624.1:c.*1204+6251C= ENSP00000501898.1:n.*1204+6251C=
ENST00000237837.1:c.315+61G= ENSP00000237837.1:n.315+61G=
NM_020638.2:c.315+61G= NP_065689.1:n.315+61G=
NM_020638.3:c.315+61G= MANE Select NP_065689.1:n.315+61G=