Canonical Allele Identifier: CA231759311
Gene: FGF23 HGNC NCBI

Linked Data

dbSNP Id: rs937411239
gnomAD v2: 12-4481884-G-A
gnomAD v3: 12-4372718-G-A
gnomAD v4: 12-4372718-G-A
MyVariant Identifiers: chr12:g.4481884G>A (hg19) chr12:g.4372718G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4372718G>A , CM000674.2:g.4372718G>A GRCh38
NC_000012.11:g.4481884G>A , CM000674.1:g.4481884G>A GRCh37
NC_000012.10:g.4352145G>A NCBI36
NG_007087.1:g.12011C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000237837.2:c.212-21C>T MANE Select ENSP00000237837.1:n.212-21C>T
ENST00000648100.1:c.*1967+6436G>A ENSP00000497536.1:n.*1967+6436G>A
ENST00000648269.1:n.1691C>T
ENST00000674624.1:c.*1204+6436G>A ENSP00000501898.1:n.*1204+6436G>A
ENST00000237837.1:c.212-21C>T ENSP00000237837.1:n.212-21C>T
NM_020638.2:c.212-21C>T NP_065689.1:n.212-21C>T
NM_020638.3:c.212-21C>T MANE Select NP_065689.1:n.212-21C>T
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