Canonical Allele Identifier: CA2617166849
Gene: FGF23 HGNC NCBI

Linked Data

gnomAD v4: 12-4372583-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4372583A>C , CM000674.2:g.4372583A>C GRCh38
NC_000012.11:g.4481749A>C , CM000674.1:g.4481749A>C GRCh37
NC_000012.10:g.4352010A>C NCBI36
NG_007087.1:g.12146T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000237837.2:c.315+11T>G MANE Select ENSP00000237837.1:n.315+11T>G
ENST00000648100.1:c.*1967+6301A>C ENSP00000497536.1:n.*1967+6301A>C
ENST00000648269.1:n.1815+11T>G
ENST00000674624.1:c.*1204+6301A>C ENSP00000501898.1:n.*1204+6301A>C
ENST00000237837.1:c.315+11T>G ENSP00000237837.1:n.315+11T>G
NM_020638.2:c.315+11T>G NP_065689.1:n.315+11T>G
NM_020638.3:c.315+11T>G MANE Select NP_065689.1:n.315+11T>G
Search 100 bp 5'
Search 100 bp 3'