Canonical Allele Identifier: CA1767395589
Gene: FGF20 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992717_16992718delinsCT , CM000670.2:g.16992717_16992718delinsCT GRCh38
NC_000008.10:g.16850226_16850227delinsCT , CM000670.1:g.16850226_16850227delinsCT GRCh37
NC_000008.9:g.16894597_16894598delinsCT NCBI36
NG_015978.1:g.14448_14449delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*354_*355delinsAG MANE Select ENSP00000180166.5:n.*354_*355delinsAG
ENST00000180166.5:c.*354_*355delinsAG ENSP00000180166.5:n.*354_*355delinsAG
NM_019851.3:c.*354_*355delinsAG MANE Select NP_062825.1:n.*354_*355delinsAG
Search 100 bp 5'
Search 100 bp 3'