Canonical Allele Identifier: CA944222963
Gene: FGF23 HGNC NCBI

Linked Data

dbSNP Id: rs1865077393
gnomAD v3: 12-4372721-A-G
gnomAD v4: 12-4372721-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4372721A>G , CM000674.2:g.4372721A>G GRCh38
NC_000012.11:g.4481887A>G , CM000674.1:g.4481887A>G GRCh37
NC_000012.10:g.4352148A>G NCBI36
NG_007087.1:g.12008T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000237837.2:c.212-24T>C MANE Select ENSP00000237837.1:n.212-24T>C
ENST00000648100.1:c.*1967+6439A>G ENSP00000497536.1:n.*1967+6439A>G
ENST00000648269.1:n.1688T>C
ENST00000674624.1:c.*1204+6439A>G ENSP00000501898.1:n.*1204+6439A>G
ENST00000237837.1:c.212-24T>C ENSP00000237837.1:n.212-24T>C
NM_020638.2:c.212-24T>C NP_065689.1:n.212-24T>C
NM_020638.3:c.212-24T>C MANE Select NP_065689.1:n.212-24T>C