Canonical Allele Identifier: CA2593751017
Gene: FGF20 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992411_16992412del , CM000670.2:g.16992411_16992412del GRCh38
NC_000008.10:g.16849920_16849921del , CM000670.1:g.16849920_16849921del GRCh37
NC_000008.9:g.16894291_16894292del NCBI36
NG_015978.1:g.14755_14756del

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*661_*662del MANE Select ENSP00000180166.5:n.*661_*662del
ENST00000180166.5:c.*661_*662del ENSP00000180166.5:n.*661_*662del
NM_019851.3:c.*661_*662del MANE Select NP_062825.1:n.*661_*662del