Canonical Allele Identifier: CA2779223987
Gene: FGF20 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992618_16992623del , CM000670.2:g.16992618_16992623del GRCh38
NC_000008.10:g.16850127_16850132del , CM000670.1:g.16850127_16850132del GRCh37
NC_000008.9:g.16894498_16894503del NCBI36
NG_015978.1:g.14543_14548del

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*449_*454del MANE Select ENSP00000180166.5:n.*449_*454del
ENST00000180166.5:c.*449_*454del ENSP00000180166.5:n.*449_*454del
NM_019851.3:c.*449_*454del MANE Select NP_062825.1:n.*449_*454del
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