Canonical Allele Identifier: CA383416773
Gene: FGF23 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.4481806C>A (hg19) chr12:g.4372640C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4372640C>A , CM000674.2:g.4372640C>A GRCh38
NC_000012.11:g.4481806C>A , CM000674.1:g.4481806C>A GRCh37
NC_000012.10:g.4352067C>A NCBI36
NG_007087.1:g.12089G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000237837.2:c.269G>T MANE Select ENSP00000237837.1:p.Ser90Ile
ENST00000648100.1:c.*1967+6358C>A ENSP00000497536.1:n.*1967+6358C>A
ENST00000648269.1:n.1769G>T
ENST00000674624.1:c.*1204+6358C>A ENSP00000501898.1:n.*1204+6358C>A
ENST00000237837.1:c.269G>T ENSP00000237837.1:p.Ser90Ile
NM_020638.2:c.269G>T NP_065689.1:p.Ser90Ile
NM_020638.3:c.269G>T MANE Select NP_065689.1:p.Ser90Ile
Search 100 bp 5'
Search 100 bp 3'