Canonical Allele Identifier: CA477950326
Gene: FGF23 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.4481811C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4372645C>G , CM000674.2:g.4372645C>G GRCh38
NC_000012.11:g.4481811C>G , CM000674.1:g.4481811C>G GRCh37
NC_000012.10:g.4352072C>G NCBI36
NG_007087.1:g.12084G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000237837.2:c.264G>C MANE Select ENSP00000237837.1:p.Val88=
ENST00000648100.1:c.*1967+6363C>G ENSP00000497536.1:n.*1967+6363C>G
ENST00000648269.1:n.1764G>C
ENST00000674624.1:c.*1204+6363C>G ENSP00000501898.1:n.*1204+6363C>G
ENST00000237837.1:c.264G>C ENSP00000237837.1:p.Val88=
NM_020638.2:c.264G>C NP_065689.1:p.Val88=
NM_020638.3:c.264G>C MANE Select NP_065689.1:p.Val88=
Search 100 bp 5'
Search 100 bp 3'