Canonical Allele Identifier: CA2779223982
Gene: FGF20 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992505T>A , CM000670.2:g.16992505T>A GRCh38
NC_000008.10:g.16850014T>A , CM000670.1:g.16850014T>A GRCh37
NC_000008.9:g.16894385T>A NCBI36
NG_015978.1:g.14661A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*567A>T MANE Select ENSP00000180166.5:n.*567A>T
ENST00000180166.5:c.*567A>T ENSP00000180166.5:n.*567A>T
NM_019851.3:c.*567A>T MANE Select NP_062825.1:n.*567A>T
Search 100 bp 5'
Search 100 bp 3'