Canonical Allele Identifier: CA1767395313
Gene: FGF20 HGNC NCBI

Linked Data

dbSNP Id: rs1809934104
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992394A>G , CM000670.2:g.16992394A>G GRCh38
NC_000008.10:g.16849903A>G , CM000670.1:g.16849903A>G GRCh37
NC_000008.9:g.16894274A>G NCBI36
NG_015978.1:g.14772T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*678T>C MANE Select ENSP00000180166.5:n.*678T>C
ENST00000180166.5:c.*678T>C ENSP00000180166.5:n.*678T>C
NM_019851.3:c.*678T>C MANE Select NP_062825.1:n.*678T>C
Search 100 bp 5'
Search 100 bp 3'