Canonical Allele Identifier: CA2686252428
Gene: FGF20 HGNC NCBI

Linked Data

gnomAD v4: 8-16992916-TGG-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992917_16992918del , CM000670.2:g.16992917_16992918del GRCh38
NC_000008.10:g.16850426_16850427del , CM000670.1:g.16850426_16850427del GRCh37
NC_000008.9:g.16894797_16894798del NCBI36
NG_015978.1:g.14248_14249del

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*154_*155del MANE Select ENSP00000180166.5:n.*154_*155del
ENST00000180166.5:c.*154_*155del ENSP00000180166.5:n.*154_*155del
NM_019851.2:c.*154_*155del NP_062825.1:n.*154_*155del
NM_019851.3:c.*154_*155del MANE Select NP_062825.1:n.*154_*155del
Search 100 bp 5'
Search 100 bp 3'