Canonical Allele Identifier: CA383416582
Gene: FGF23 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.4481759C>A (hg19) chr12:g.4372593C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4372593C>A , CM000674.2:g.4372593C>A GRCh38
NC_000012.11:g.4481759C>A , CM000674.1:g.4481759C>A GRCh37
NC_000012.10:g.4352020C>A NCBI36
NG_007087.1:g.12136G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000237837.2:c.315+1G>T MANE Select ENSP00000237837.1:n.315+1G>T
ENST00000648100.1:c.*1967+6311C>A ENSP00000497536.1:n.*1967+6311C>A
ENST00000648269.1:n.1815+1G>T
ENST00000674624.1:c.*1204+6311C>A ENSP00000501898.1:n.*1204+6311C>A
ENST00000237837.1:c.315+1G>T ENSP00000237837.1:n.315+1G>T
NM_020638.2:c.315+1G>T NP_065689.1:n.315+1G>T
NM_020638.3:c.315+1G>T MANE Select NP_065689.1:n.315+1G>T
Search 100 bp 5'
Search 100 bp 3'