Canonical Allele Identifier: CA2686252328
Gene: FGF20 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992817del , CM000670.2:g.16992817del GRCh38
NC_000008.10:g.16850326del , CM000670.1:g.16850326del GRCh37
NC_000008.9:g.16894697del NCBI36
NG_015978.1:g.14353del

Transcript Alleles

HGVS Amino-acid change
ENST00000180166.6:c.*259del MANE Select ENSP00000180166.5:n.*259del
ENST00000180166.5:c.*259del ENSP00000180166.5:n.*259del
NM_019851.3:c.*259del MANE Select NP_062825.1:n.*259del