Canonical Allele Identifier: CA1767395689
Gene: FGF20 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992840C= , CM000670.2:g.16992840C= GRCh38
NC_000008.10:g.16850349C= , CM000670.1:g.16850349C= GRCh37
NC_000008.9:g.16894720C= NCBI36
NG_015978.1:g.14326G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*232G= MANE Select ENSP00000180166.5:n.*232G=
ENST00000180166.5:c.*232G= ENSP00000180166.5:n.*232G=
NM_019851.2:c.*232G= NP_062825.1:n.*232G=
NM_019851.3:c.*232G= MANE Select NP_062825.1:n.*232G=
Search 100 bp 5'
Search 100 bp 3'