Canonical Allele Identifier: CA2686252505
Gene: FGF20 HGNC NCBI

Linked Data

gnomAD v4: 8-16992992-T-TGGGTCATTA
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992993_16993001dup , CM000670.2:g.16992993_16993001dup GRCh38
NC_000008.10:g.16850502_16850510dup , CM000670.1:g.16850502_16850510dup GRCh37
NC_000008.9:g.16894873_16894881dup NCBI36
NG_015978.1:g.14165_14173dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*71_*79dup MANE Select ENSP00000180166.5:n.*71_*79dup
ENST00000180166.5:c.*71_*79dup ENSP00000180166.5:n.*71_*79dup
ENST00000519941.1:c.411_419dup
NM_019851.2:c.*71_*79dup NP_062825.1:n.*71_*79dup
NM_019851.3:c.*71_*79dup MANE Select NP_062825.1:n.*71_*79dup
Search 100 bp 5'
Search 100 bp 3'