Canonical Allele Identifier: CA2686252487
Gene: FGF20 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992975del , CM000670.2:g.16992975del GRCh38
NC_000008.10:g.16850484del , CM000670.1:g.16850484del GRCh37
NC_000008.9:g.16894855del NCBI36
NG_015978.1:g.14191del

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*97del MANE Select ENSP00000180166.5:n.*97del
ENST00000180166.5:c.*97del ENSP00000180166.5:n.*97del
NM_019851.2:c.*97del NP_062825.1:n.*97del
NM_019851.3:c.*97del MANE Select NP_062825.1:n.*97del