Canonical Allele Identifier: CA2013130429
Gene: FGF23 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4372721A= , CM000674.2:g.4372721A= GRCh38
NC_000012.11:g.4481887A= , CM000674.1:g.4481887A= GRCh37
NC_000012.10:g.4352148A= NCBI36
NG_007087.1:g.12008T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000237837.2:c.212-24T= MANE Select ENSP00000237837.1:n.212-24T=
ENST00000648100.1:c.*1967+6439A= ENSP00000497536.1:n.*1967+6439A=
ENST00000648269.1:n.1688T=
ENST00000674624.1:c.*1204+6439A= ENSP00000501898.1:n.*1204+6439A=
ENST00000237837.1:c.212-24T= ENSP00000237837.1:n.212-24T=
NM_020638.2:c.212-24T= NP_065689.1:n.212-24T=
NM_020638.3:c.212-24T= MANE Select NP_065689.1:n.212-24T=
Search 100 bp 5'
Search 100 bp 3'