Canonical Allele Identifier: CA2540198215
Gene: FGF20 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992819del , CM000670.2:g.16992819del GRCh38
NC_000008.10:g.16850328del , CM000670.1:g.16850328del GRCh37
NC_000008.9:g.16894699del NCBI36
NG_015978.1:g.14348del

Transcript Alleles

HGVS Amino-acid change
ENST00000180166.6:c.*254del MANE Select ENSP00000180166.5:n.*254del
ENST00000180166.5:c.*254del ENSP00000180166.5:n.*254del
NM_019851.3:c.*254del MANE Select NP_062825.1:n.*254del