Canonical Allele Identifier: CA1767395683
Gene: FGF20 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992838G= , CM000670.2:g.16992838G= GRCh38
NC_000008.10:g.16850347G= , CM000670.1:g.16850347G= GRCh37
NC_000008.9:g.16894718G= NCBI36
NG_015978.1:g.14328C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*234C= MANE Select ENSP00000180166.5:n.*234C=
ENST00000180166.5:c.*234C= ENSP00000180166.5:n.*234C=
NM_019851.2:c.*234C= NP_062825.1:n.*234C=
NM_019851.3:c.*234C= MANE Select NP_062825.1:n.*234C=