Canonical Allele Identifier: CA2686252321
Gene: FGF20 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992806dup , CM000670.2:g.16992806dup GRCh38
NC_000008.10:g.16850315dup , CM000670.1:g.16850315dup GRCh37
NC_000008.9:g.16894686dup NCBI36
NG_015978.1:g.14362dup

Transcript Alleles

HGVS Amino-acid change
ENST00000180166.6:c.*268dup MANE Select ENSP00000180166.5:n.*268dup
ENST00000180166.5:c.*268dup ENSP00000180166.5:n.*268dup
NM_019851.3:c.*268dup MANE Select NP_062825.1:n.*268dup