Canonical Allele Identifier: CA849279900

Gene: FGF20

Linked Data

• dbSNP Id: rs1307171925
• gnomAD v3: 8-16992619-A-G
• gnomAD v4: 8-16992619-A-G
• MyVariant Identifiers: chr8:g.16850128A>G (hg19) ; chr8:g.16992619A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.16992619A>G , CM000670.2:g.16992619A>G	GRCh38
NC_000008.10:g.16850128A>G , CM000670.1:g.16850128A>G	GRCh37
NC_000008.9:g.16894499A>G	NCBI36
NG_015978.1:g.14547T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000180166.6:c.*453T>C MANE Select	ENSP00000180166.5:n.*453T>C
ENST00000180166.5:c.*453T>C	ENSP00000180166.5:n.*453T>C
NM_019851.3:c.*453T>C MANE Select	NP_062825.1:n.*453T>C