Canonical Allele Identifier: CA2013130373
Gene: FGF23 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4372567G= , CM000674.2:g.4372567G= GRCh38
NC_000012.11:g.4481733G= , CM000674.1:g.4481733G= GRCh37
NC_000012.10:g.4351994G= NCBI36
NG_007087.1:g.12162C=

Transcript Alleles

HGVS Amino-acid change
ENST00000237837.2:c.315+27C= MANE Select ENSP00000237837.1:n.315+27C=
ENST00000648100.1:c.*1967+6285G= ENSP00000497536.1:n.*1967+6285G=
ENST00000648269.1:n.1815+27C=
ENST00000674624.1:c.*1204+6285G= ENSP00000501898.1:n.*1204+6285G=
ENST00000237837.1:c.315+27C= ENSP00000237837.1:n.315+27C=
NM_020638.2:c.315+27C= NP_065689.1:n.315+27C=
NM_020638.3:c.315+27C= MANE Select NP_065689.1:n.315+27C=
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