Canonical Allele Identifier: CA1767395665
Gene: FGF20 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992825G= , CM000670.2:g.16992825G= GRCh38
NC_000008.10:g.16850334G= , CM000670.1:g.16850334G= GRCh37
NC_000008.9:g.16894705G= NCBI36
NG_015978.1:g.14341C=

Transcript Alleles

HGVS Amino-acid change
ENST00000180166.6:c.*247C= MANE Select ENSP00000180166.5:n.*247C=
ENST00000180166.5:c.*247C= ENSP00000180166.5:n.*247C=
NM_019851.2:c.*247C= NP_062825.1:n.*247C=
NM_019851.3:c.*247C= MANE Select NP_062825.1:n.*247C=