Canonical Allele Identifier: CA2779223989
Gene: FGF20 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992624_16992625insTT , CM000670.2:g.16992624_16992625insTT GRCh38
NC_000008.10:g.16850133_16850134insTT , CM000670.1:g.16850133_16850134insTT GRCh37
NC_000008.9:g.16894504_16894505insTT NCBI36
NG_015978.1:g.14542_14543insAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*448_*449insAA MANE Select ENSP00000180166.5:n.*448_*449insAA
ENST00000180166.5:c.*448_*449insAA ENSP00000180166.5:n.*448_*449insAA
NM_019851.3:c.*448_*449insAA MANE Select NP_062825.1:n.*448_*449insAA