Canonical Allele Identifier: CA2686252450
Gene: FGF20 HGNC NCBI

Linked Data

gnomAD v4: 8-16992935-TC-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992936del , CM000670.2:g.16992936del GRCh38
NC_000008.10:g.16850445del , CM000670.1:g.16850445del GRCh37
NC_000008.9:g.16894816del NCBI36
NG_015978.1:g.14230del

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*136del MANE Select ENSP00000180166.5:n.*136del
ENST00000180166.5:c.*136del ENSP00000180166.5:n.*136del
NM_019851.2:c.*136del NP_062825.1:n.*136del
NM_019851.3:c.*136del MANE Select NP_062825.1:n.*136del
Search 100 bp 5'
Search 100 bp 3'