Canonical Allele Identifier: CA603043732
Gene: FGF23 HGNC NCBI

Linked Data

dbSNP Id: rs1394556064
gnomAD v2: 12-4481736-G-C
MyVariant Identifiers: chr12:g.4481736G>C (hg19) chr12:g.4372570G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4372570G>C , CM000674.2:g.4372570G>C GRCh38
NC_000012.11:g.4481736G>C , CM000674.1:g.4481736G>C GRCh37
NC_000012.10:g.4351997G>C NCBI36
NG_007087.1:g.12159C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000237837.2:c.315+24C>G MANE Select ENSP00000237837.1:n.315+24C>G
ENST00000648100.1:c.*1967+6288G>C ENSP00000497536.1:n.*1967+6288G>C
ENST00000648269.1:n.1815+24C>G
ENST00000674624.1:c.*1204+6288G>C ENSP00000501898.1:n.*1204+6288G>C
ENST00000237837.1:c.315+24C>G ENSP00000237837.1:n.315+24C>G
NM_020638.2:c.315+24C>G NP_065689.1:n.315+24C>G
NM_020638.3:c.315+24C>G MANE Select NP_065689.1:n.315+24C>G
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