Canonical Allele Identifier: CA383416800
Gene: FGF23 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.4481812A>T (hg19) chr12:g.4372646A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4372646A>T , CM000674.2:g.4372646A>T GRCh38
NC_000012.11:g.4481812A>T , CM000674.1:g.4481812A>T GRCh37
NC_000012.10:g.4352073A>T NCBI36
NG_007087.1:g.12083T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000237837.2:c.263T>A MANE Select ENSP00000237837.1:p.Val88Glu
ENST00000648100.1:c.*1967+6364A>T ENSP00000497536.1:n.*1967+6364A>T
ENST00000648269.1:n.1763T>A
ENST00000674624.1:c.*1204+6364A>T ENSP00000501898.1:n.*1204+6364A>T
ENST00000237837.1:c.263T>A ENSP00000237837.1:p.Val88Glu
NM_020638.2:c.263T>A NP_065689.1:p.Val88Glu
NM_020638.3:c.263T>A MANE Select NP_065689.1:p.Val88Glu
Search 100 bp 5'
Search 100 bp 3'