Canonical Allele Identifier: CA231759227
Gene: FGF23 HGNC NCBI

Linked Data

dbSNP Id: rs12426118
MyVariant Identifiers: chr12:g.4481793G>A (hg19) chr12:g.4372627G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4372627G>A , CM000674.2:g.4372627G>A GRCh38
NC_000012.11:g.4481793G>A , CM000674.1:g.4481793G>A GRCh37
NC_000012.10:g.4352054G>A NCBI36
NG_007087.1:g.12102C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000237837.2:c.282C>T MANE Select ENSP00000237837.1:p.Leu94=
ENST00000648100.1:c.*1967+6345G>A ENSP00000497536.1:n.*1967+6345G>A
ENST00000648269.1:n.1782C>T
ENST00000674624.1:c.*1204+6345G>A ENSP00000501898.1:n.*1204+6345G>A
ENST00000237837.1:c.282C>T ENSP00000237837.1:p.Leu94=
NM_020638.2:c.282C>T NP_065689.1:p.Leu94=
NM_020638.3:c.282C>T MANE Select NP_065689.1:p.Leu94=
Search 100 bp 5'
Search 100 bp 3'