Canonical Allele Identifier: CA603043733

Gene: FGF23

Linked Data

• dbSNP Id: rs1429198452
• gnomAD v2: 12-4481739-C-T
• gnomAD v4: 12-4372573-C-T
• MyVariant Identifiers: chr12:g.4481739C>T (hg19) ; chr12:g.4372573C>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000237837.2:c.315+21G>A MANE Select	ENSP00000237837.1:n.315+21G>A
ENST00000648100.1:c.*1967+6291C>T	ENSP00000497536.1:n.*1967+6291C>T
ENST00000648269.1:n.1815+21G>A
ENST00000674624.1:c.*1204+6291C>T	ENSP00000501898.1:n.*1204+6291C>T
ENST00000237837.1:c.315+21G>A	ENSP00000237837.1:n.315+21G>A
NM_020638.2:c.315+21G>A	NP_065689.1:n.315+21G>A
NM_020638.3:c.315+21G>A MANE Select	NP_065689.1:n.315+21G>A