Canonical Allele Identifier: CA383416802
Gene: FGF23 HGNC NCBI

Linked Data

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

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

Transcript Alleles

HGVS Amino-acid change
ENST00000237837.2:c.262G>T MANE Select ENSP00000237837.1:p.Val88Leu
ENST00000648100.1:c.*1967+6365C>A ENSP00000497536.1:n.*1967+6365C>A
ENST00000648269.1:n.1762G>T
ENST00000674624.1:c.*1204+6365C>A ENSP00000501898.1:n.*1204+6365C>A
ENST00000237837.1:c.262G>T ENSP00000237837.1:p.Val88Leu
NM_020638.2:c.262G>T NP_065689.1:p.Val88Leu
NM_020638.3:c.262G>T MANE Select NP_065689.1:p.Val88Leu
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Search 100 bp 3'