Canonical Allele Identifier: CA2013130399
Gene: FGF23 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4372648A= , CM000674.2:g.4372648A= GRCh38
NC_000012.11:g.4481814A= , CM000674.1:g.4481814A= GRCh37
NC_000012.10:g.4352075A= NCBI36
NG_007087.1:g.12081T=

Transcript Alleles

HGVS Amino-acid change
ENST00000237837.2:c.261T= MANE Select ENSP00000237837.1:p.Gly87=
ENST00000648100.1:c.*1967+6366A= ENSP00000497536.1:n.*1967+6366A=
ENST00000648269.1:n.1761T=
ENST00000674624.1:c.*1204+6366A= ENSP00000501898.1:n.*1204+6366A=
ENST00000237837.1:c.261T= ENSP00000237837.1:p.Gly87=
NM_020638.2:c.261T= NP_065689.1:p.Gly87=
NM_020638.3:c.261T= MANE Select NP_065689.1:p.Gly87=