Canonical Allele Identifier: CA2013130437
Gene: FGF23 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4372737C= , CM000674.2:g.4372737C= GRCh38
NC_000012.11:g.4481903C= , CM000674.1:g.4481903C= GRCh37
NC_000012.10:g.4352164C= NCBI36
NG_007087.1:g.11992G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000237837.2:c.212-40G= MANE Select ENSP00000237837.1:n.212-40G=
ENST00000648100.1:c.*1967+6455C= ENSP00000497536.1:n.*1967+6455C=
ENST00000648269.1:n.1672G=
ENST00000674624.1:c.*1204+6455C= ENSP00000501898.1:n.*1204+6455C=
ENST00000237837.1:c.212-40G= ENSP00000237837.1:n.212-40G=
NM_020638.2:c.212-40G= NP_065689.1:n.212-40G=
NM_020638.3:c.212-40G= MANE Select NP_065689.1:n.212-40G=
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