Canonical Allele Identifier: CA1767395601
Gene: FGF20 HGNC NCBI

Linked Data

dbSNP Id: rs1809943027

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992730A>C , CM000670.2:g.16992730A>C GRCh38
NC_000008.10:g.16850239A>C , CM000670.1:g.16850239A>C GRCh37
NC_000008.9:g.16894610A>C NCBI36
NG_015978.1:g.14436T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*342T>G MANE Select ENSP00000180166.5:n.*342T>G
ENST00000180166.5:c.*342T>G ENSP00000180166.5:n.*342T>G
NM_019851.3:c.*342T>G MANE Select NP_062825.1:n.*342T>G