Canonical Allele Identifier: CA477950265
Gene: FGF23 HGNC NCBI

Linked Data

ClinVar Variation Id: 2778835
ClinVar RCV Id: RCV003661730
MyVariant Identifiers: chr12:g.4481763T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4372597T>A , CM000674.2:g.4372597T>A GRCh38
NC_000012.11:g.4481763T>A , CM000674.1:g.4481763T>A GRCh37
NC_000012.10:g.4352024T>A NCBI36
NG_007087.1:g.12132A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000237837.2:c.312A>T MANE Select ENSP00000237837.1:p.Gly104=
ENST00000648100.1:c.*1967+6315T>A ENSP00000497536.1:n.*1967+6315T>A
ENST00000648269.1:n.1812A>T
ENST00000674624.1:c.*1204+6315T>A ENSP00000501898.1:n.*1204+6315T>A
ENST00000237837.1:c.312A>T ENSP00000237837.1:p.Gly104=
NM_020638.2:c.312A>T NP_065689.1:p.Gly104=
NM_020638.3:c.312A>T MANE Select NP_065689.1:p.Gly104=
Search 100 bp 5'
Search 100 bp 3'