Canonical Allele Identifier: CA689061869

Gene: FGF23

Linked Data

• dbSNP Id: rs1473388653
• gnomAD v3: 12-4372528-T-G
• gnomAD v4: 12-4372528-T-G
• MyVariant Identifiers: chr12:g.4481694T>G (hg19) ; chr12:g.4372528T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.4372528T>G , CM000674.2:g.4372528T>G	GRCh38
NC_000012.11:g.4481694T>G , CM000674.1:g.4481694T>G	GRCh37
NC_000012.10:g.4351955T>G	NCBI36
NG_007087.1:g.12201A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000237837.2:c.315+66A>C MANE Select	ENSP00000237837.1:n.315+66A>C
ENST00000648100.1:c.*1967+6246T>G	ENSP00000497536.1:n.*1967+6246T>G
ENST00000648269.1:n.1815+66A>C
ENST00000674624.1:c.*1204+6246T>G	ENSP00000501898.1:n.*1204+6246T>G
ENST00000237837.1:c.315+66A>C	ENSP00000237837.1:n.315+66A>C
NM_020638.2:c.315+66A>C	NP_065689.1:n.315+66A>C
NM_020638.3:c.315+66A>C MANE Select	NP_065689.1:n.315+66A>C