Canonical Allele Identifier: CA2779224014
Gene: FGF20 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992929_16992930del , CM000670.2:g.16992929_16992930del GRCh38
NC_000008.10:g.16850438_16850439del , CM000670.1:g.16850438_16850439del GRCh37
NC_000008.9:g.16894809_16894810del NCBI36
NG_015978.1:g.14236_14237del

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*142_*143del MANE Select ENSP00000180166.5:n.*142_*143del
ENST00000180166.5:c.*142_*143del ENSP00000180166.5:n.*142_*143del
NM_019851.2:c.*142_*143del NP_062825.1:n.*142_*143del
NM_019851.3:c.*142_*143del MANE Select NP_062825.1:n.*142_*143del
Search 100 bp 5'
Search 100 bp 3'