Canonical Allele Identifier: CA2013130379
Gene: FGF23 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4372575A= , CM000674.2:g.4372575A= GRCh38
NC_000012.11:g.4481741A= , CM000674.1:g.4481741A= GRCh37
NC_000012.10:g.4352002A= NCBI36
NG_007087.1:g.12154T=

Transcript Alleles

HGVS Amino-acid change
ENST00000237837.2:c.315+19T= MANE Select ENSP00000237837.1:n.315+19T=
ENST00000648100.1:c.*1967+6293A= ENSP00000497536.1:n.*1967+6293A=
ENST00000648269.1:n.1815+19T=
ENST00000674624.1:c.*1204+6293A= ENSP00000501898.1:n.*1204+6293A=
ENST00000237837.1:c.315+19T= ENSP00000237837.1:n.315+19T=
NM_020638.2:c.315+19T= NP_065689.1:n.315+19T=
NM_020638.3:c.315+19T= MANE Select NP_065689.1:n.315+19T=
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