Canonical Allele Identifier: CA2617166831
Gene: FGF23 HGNC NCBI

Linked Data

gnomAD v4: 12-4372536-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4372536G>A , CM000674.2:g.4372536G>A GRCh38
NC_000012.11:g.4481702G>A , CM000674.1:g.4481702G>A GRCh37
NC_000012.10:g.4351963G>A NCBI36
NG_007087.1:g.12193C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000237837.2:c.315+58C>T MANE Select ENSP00000237837.1:n.315+58C>T
ENST00000648100.1:c.*1967+6254G>A ENSP00000497536.1:n.*1967+6254G>A
ENST00000648269.1:n.1815+58C>T
ENST00000674624.1:c.*1204+6254G>A ENSP00000501898.1:n.*1204+6254G>A
ENST00000237837.1:c.315+58C>T ENSP00000237837.1:n.315+58C>T
NM_020638.2:c.315+58C>T NP_065689.1:n.315+58C>T
NM_020638.3:c.315+58C>T MANE Select NP_065689.1:n.315+58C>T