Canonical Allele Identifier: CA2779224009
Gene: FGF20 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992921_16992939del , CM000670.2:g.16992921_16992939del GRCh38
NC_000008.10:g.16850430_16850448del , CM000670.1:g.16850430_16850448del GRCh37
NC_000008.9:g.16894801_16894819del NCBI36
NG_015978.1:g.14229_14247del

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*135_*153del MANE Select ENSP00000180166.5:n.*135_*153del
ENST00000180166.5:c.*135_*153del ENSP00000180166.5:n.*135_*153del
NM_019851.2:c.*135_*153del NP_062825.1:n.*135_*153del
NM_019851.3:c.*135_*153del MANE Select NP_062825.1:n.*135_*153del
Search 100 bp 5'
Search 100 bp 3'