Canonical Allele Identifier: CA1767395618
Gene: FGF20 HGNC NCBI

Linked Data

dbSNP Id: rs1809943308
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992746A>T , CM000670.2:g.16992746A>T GRCh38
NC_000008.10:g.16850255A>T , CM000670.1:g.16850255A>T GRCh37
NC_000008.9:g.16894626A>T NCBI36
NG_015978.1:g.14420T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*326T>A MANE Select ENSP00000180166.5:n.*326T>A
ENST00000180166.5:c.*326T>A ENSP00000180166.5:n.*326T>A
NM_019851.3:c.*326T>A MANE Select NP_062825.1:n.*326T>A
Search 100 bp 5'
Search 100 bp 3'