Canonical Allele Identifier: CA383416674
Gene: FGF23 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.4481783A>C (hg19) chr12:g.4372617A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4372617A>C , CM000674.2:g.4372617A>C GRCh38
NC_000012.11:g.4481783A>C , CM000674.1:g.4481783A>C GRCh37
NC_000012.10:g.4352044A>C NCBI36
NG_007087.1:g.12112T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000237837.2:c.292T>G MANE Select ENSP00000237837.1:p.Phe98Val
ENST00000648100.1:c.*1967+6335A>C ENSP00000497536.1:n.*1967+6335A>C
ENST00000648269.1:n.1792T>G
ENST00000674624.1:c.*1204+6335A>C ENSP00000501898.1:n.*1204+6335A>C
ENST00000237837.1:c.292T>G ENSP00000237837.1:p.Phe98Val
NM_020638.2:c.292T>G NP_065689.1:p.Phe98Val
NM_020638.3:c.292T>G MANE Select NP_065689.1:p.Phe98Val
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Search 100 bp 3'