Canonical Allele Identifier: CA2013130378
Gene: FGF23 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4372573C= , CM000674.2:g.4372573C= GRCh38
NC_000012.11:g.4481739C= , CM000674.1:g.4481739C= GRCh37
NC_000012.10:g.4352000C= NCBI36
NG_007087.1:g.12156G=

Transcript Alleles

HGVS Amino-acid change
ENST00000237837.2:c.315+21G= MANE Select ENSP00000237837.1:n.315+21G=
ENST00000648100.1:c.*1967+6291C= ENSP00000497536.1:n.*1967+6291C=
ENST00000648269.1:n.1815+21G=
ENST00000674624.1:c.*1204+6291C= ENSP00000501898.1:n.*1204+6291C=
ENST00000237837.1:c.315+21G= ENSP00000237837.1:n.315+21G=
NM_020638.2:c.315+21G= NP_065689.1:n.315+21G=
NM_020638.3:c.315+21G= MANE Select NP_065689.1:n.315+21G=
Search 100 bp 5'
Search 100 bp 3'