Canonical Allele Identifier: CA2686252429
Gene: FGF20 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992917_16992918insT , CM000670.2:g.16992917_16992918insT GRCh38
NC_000008.10:g.16850426_16850427insT , CM000670.1:g.16850426_16850427insT GRCh37
NC_000008.9:g.16894797_16894798insT NCBI36
NG_015978.1:g.14248_14249insA

Transcript Alleles

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