Canonical Allele Identifier: CA2617166840
Gene: FGF23 HGNC NCBI

Linked Data

gnomAD v4: 12-4372557-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4372557G>A , CM000674.2:g.4372557G>A GRCh38
NC_000012.11:g.4481723G>A , CM000674.1:g.4481723G>A GRCh37
NC_000012.10:g.4351984G>A NCBI36
NG_007087.1:g.12172C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000237837.2:c.315+37C>T MANE Select ENSP00000237837.1:n.315+37C>T
ENST00000648100.1:c.*1967+6275G>A ENSP00000497536.1:n.*1967+6275G>A
ENST00000648269.1:n.1815+37C>T
ENST00000674624.1:c.*1204+6275G>A ENSP00000501898.1:n.*1204+6275G>A
ENST00000237837.1:c.315+37C>T ENSP00000237837.1:n.315+37C>T
NM_020638.2:c.315+37C>T NP_065689.1:n.315+37C>T
NM_020638.3:c.315+37C>T MANE Select NP_065689.1:n.315+37C>T