Canonical Allele Identifier: CA2686252344
Gene: FGF20 HGNC NCBI

Linked Data

gnomAD v4: 8-16992833-GT-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992834del , CM000670.2:g.16992834del GRCh38
NC_000008.10:g.16850343del , CM000670.1:g.16850343del GRCh37
NC_000008.9:g.16894714del NCBI36
NG_015978.1:g.14332del

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*238del MANE Select ENSP00000180166.5:n.*238del
ENST00000180166.5:c.*238del ENSP00000180166.5:n.*238del
NM_019851.2:c.*238del NP_062825.1:n.*238del
NM_019851.3:c.*238del MANE Select NP_062825.1:n.*238del
Search 100 bp 5'
Search 100 bp 3'