Canonical Allele Identifier: CA2779224008
Gene: FGF20 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992881A>C , CM000670.2:g.16992881A>C GRCh38
NC_000008.10:g.16850390A>C , CM000670.1:g.16850390A>C GRCh37
NC_000008.9:g.16894761A>C NCBI36
NG_015978.1:g.14285T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*191T>G MANE Select ENSP00000180166.5:n.*191T>G
ENST00000180166.5:c.*191T>G ENSP00000180166.5:n.*191T>G
NM_019851.2:c.*191T>G NP_062825.1:n.*191T>G
NM_019851.3:c.*191T>G MANE Select NP_062825.1:n.*191T>G