Canonical Allele Identifier: CA2617166835
Gene: FGF23 HGNC NCBI

Linked Data

gnomAD v4: 12-4372547-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4372547T>G , CM000674.2:g.4372547T>G GRCh38
NC_000012.11:g.4481713T>G , CM000674.1:g.4481713T>G GRCh37
NC_000012.10:g.4351974T>G NCBI36
NG_007087.1:g.12182A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000237837.2:c.315+47A>C MANE Select ENSP00000237837.1:n.315+47A>C
ENST00000648100.1:c.*1967+6265T>G ENSP00000497536.1:n.*1967+6265T>G
ENST00000648269.1:n.1815+47A>C
ENST00000674624.1:c.*1204+6265T>G ENSP00000501898.1:n.*1204+6265T>G
ENST00000237837.1:c.315+47A>C ENSP00000237837.1:n.315+47A>C
NM_020638.2:c.315+47A>C NP_065689.1:n.315+47A>C
NM_020638.3:c.315+47A>C MANE Select NP_065689.1:n.315+47A>C
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