Canonical Allele Identifier: CA383416672

Gene: FGF23

Linked Data

• MyVariant Identifiers: chr12:g.4481782A>T (hg19) ; chr12:g.4372616A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.4372616A>T , CM000674.2:g.4372616A>T	GRCh38
NC_000012.11:g.4481782A>T , CM000674.1:g.4481782A>T	GRCh37
NC_000012.10:g.4352043A>T	NCBI36
NG_007087.1:g.12113T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237837.2:c.293T>A MANE Select	ENSP00000237837.1:p.Phe98Tyr
ENST00000648100.1:c.*1967+6334A>T	ENSP00000497536.1:n.*1967+6334A>T
ENST00000648269.1:n.1793T>A
ENST00000674624.1:c.*1204+6334A>T	ENSP00000501898.1:n.*1204+6334A>T
ENST00000237837.1:c.293T>A	ENSP00000237837.1:p.Phe98Tyr
NM_020638.2:c.293T>A	NP_065689.1:p.Phe98Tyr
NM_020638.3:c.293T>A MANE Select	NP_065689.1:p.Phe98Tyr