Canonical Allele Identifier: CA849280108

Gene: FGF20

Linked Data

• dbSNP Id: rs746261060
• gnomAD v3: 8-16992908-A-G
• gnomAD v4: 8-16992908-A-G
• MyVariant Identifiers: chr8:g.16850417A>G (hg19) ; chr8:g.16992908A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.16992908A>G , CM000670.2:g.16992908A>G	GRCh38
NC_000008.10:g.16850417A>G , CM000670.1:g.16850417A>G	GRCh37
NC_000008.9:g.16894788A>G	NCBI36
NG_015978.1:g.14258T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000180166.6:c.*164T>C MANE Select	ENSP00000180166.5:n.*164T>C
ENST00000180166.5:c.*164T>C	ENSP00000180166.5:n.*164T>C
NM_019851.2:c.*164T>C	NP_062825.1:n.*164T>C
NM_019851.3:c.*164T>C MANE Select	NP_062825.1:n.*164T>C