Canonical Allele Identifier: CA2686252430
Gene: FGF20 HGNC NCBI

Linked Data

gnomAD v4: 8-16992917-G-GTT
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992917_16992918insTT , CM000670.2:g.16992917_16992918insTT GRCh38
NC_000008.10:g.16850426_16850427insTT , CM000670.1:g.16850426_16850427insTT GRCh37
NC_000008.9:g.16894797_16894798insTT NCBI36
NG_015978.1:g.14248_14249insAA

Transcript Alleles

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