Canonical Allele Identifier: CA2593751024
Gene: FGF20 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992929_16992931del , CM000670.2:g.16992929_16992931del GRCh38
NC_000008.10:g.16850438_16850440del , CM000670.1:g.16850438_16850440del GRCh37
NC_000008.9:g.16894809_16894811del NCBI36
NG_015978.1:g.14235_14237del

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*141_*143del MANE Select ENSP00000180166.5:n.*141_*143del
ENST00000180166.5:c.*141_*143del ENSP00000180166.5:n.*141_*143del
NM_019851.2:c.*141_*143del NP_062825.1:n.*141_*143del
NM_019851.3:c.*141_*143del MANE Select NP_062825.1:n.*141_*143del