Canonical Allele Identifier: CA2686252184
Gene: FGF20 HGNC NCBI

Linked Data

gnomAD v4: 8-16992614-TC-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992615del , CM000670.2:g.16992615del GRCh38
NC_000008.10:g.16850124del , CM000670.1:g.16850124del GRCh37
NC_000008.9:g.16894495del NCBI36
NG_015978.1:g.14551del

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*457del MANE Select ENSP00000180166.5:n.*457del
ENST00000180166.5:c.*457del ENSP00000180166.5:n.*457del
NM_019851.3:c.*457del MANE Select NP_062825.1:n.*457del
Search 100 bp 5'
Search 100 bp 3'