Canonical Allele Identifier: CA477950328
Gene: FGF23 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.4481814A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4372648A>C , CM000674.2:g.4372648A>C GRCh38
NC_000012.11:g.4481814A>C , CM000674.1:g.4481814A>C GRCh37
NC_000012.10:g.4352075A>C NCBI36
NG_007087.1:g.12081T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000237837.2:c.261T>G MANE Select ENSP00000237837.1:p.Gly87=
ENST00000648100.1:c.*1967+6366A>C ENSP00000497536.1:n.*1967+6366A>C
ENST00000648269.1:n.1761T>G
ENST00000674624.1:c.*1204+6366A>C ENSP00000501898.1:n.*1204+6366A>C
ENST00000237837.1:c.261T>G ENSP00000237837.1:p.Gly87=
NM_020638.2:c.261T>G NP_065689.1:p.Gly87=
NM_020638.3:c.261T>G MANE Select NP_065689.1:p.Gly87=
Search 100 bp 5'
Search 100 bp 3'