Canonical Allele Identifier: CA2013130377
Gene: FGF23 HGNC NCBI

Linked Data

dbSNP Id: rs1565456699
gnomAD v4: 12-4372572-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4372572C>T , CM000674.2:g.4372572C>T GRCh38
NC_000012.11:g.4481738C>T , CM000674.1:g.4481738C>T GRCh37
NC_000012.10:g.4351999C>T NCBI36
NG_007087.1:g.12157G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000237837.2:c.315+22G>A MANE Select ENSP00000237837.1:n.315+22G>A
ENST00000648100.1:c.*1967+6290C>T ENSP00000497536.1:n.*1967+6290C>T
ENST00000648269.1:n.1815+22G>A
ENST00000674624.1:c.*1204+6290C>T ENSP00000501898.1:n.*1204+6290C>T
ENST00000237837.1:c.315+22G>A ENSP00000237837.1:n.315+22G>A
NM_020638.2:c.315+22G>A NP_065689.1:n.315+22G>A
NM_020638.3:c.315+22G>A MANE Select NP_065689.1:n.315+22G>A
Search 100 bp 5'
Search 100 bp 3'