Canonical Allele Identifier: CA383416661

Gene: FGF23

Linked Data

• MyVariant Identifiers: chr12:g.4481779C>T (hg19) ; chr12:g.4372613C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.4372613C>T , CM000674.2:g.4372613C>T	GRCh38
NC_000012.11:g.4481779C>T , CM000674.1:g.4481779C>T	GRCh37
NC_000012.10:g.4352040C>T	NCBI36
NG_007087.1:g.12116G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237837.2:c.296G>A MANE Select	ENSP00000237837.1:p.Arg99Lys
ENST00000648100.1:c.*1967+6331C>T	ENSP00000497536.1:n.*1967+6331C>T
ENST00000648269.1:n.1796G>A
ENST00000674624.1:c.*1204+6331C>T	ENSP00000501898.1:n.*1204+6331C>T
ENST00000237837.1:c.296G>A	ENSP00000237837.1:p.Arg99Lys
NM_020638.2:c.296G>A	NP_065689.1:p.Arg99Lys
NM_020638.3:c.296G>A MANE Select	NP_065689.1:p.Arg99Lys