Canonical Allele Identifier: CA383416805
Gene: FGF23 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.4481813C>T (hg19) chr12:g.4372647C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4372647C>T , CM000674.2:g.4372647C>T GRCh38
NC_000012.11:g.4481813C>T , CM000674.1:g.4481813C>T GRCh37
NC_000012.10:g.4352074C>T NCBI36
NG_007087.1:g.12082G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000237837.2:c.262G>A MANE Select ENSP00000237837.1:p.Val88Met
ENST00000648100.1:c.*1967+6365C>T ENSP00000497536.1:n.*1967+6365C>T
ENST00000648269.1:n.1762G>A
ENST00000674624.1:c.*1204+6365C>T ENSP00000501898.1:n.*1204+6365C>T
ENST00000237837.1:c.262G>A ENSP00000237837.1:p.Val88Met
NM_020638.2:c.262G>A NP_065689.1:p.Val88Met
NM_020638.3:c.262G>A MANE Select NP_065689.1:p.Val88Met
Search 100 bp 5'
Search 100 bp 3'