Canonical Allele Identifier: CA1767395692
Gene: FGF20 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992841T= , CM000670.2:g.16992841T= GRCh38
NC_000008.10:g.16850350T= , CM000670.1:g.16850350T= GRCh37
NC_000008.9:g.16894721T= NCBI36
NG_015978.1:g.14325A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*231A= MANE Select ENSP00000180166.5:n.*231A=
ENST00000180166.5:c.*231A= ENSP00000180166.5:n.*231A=
NM_019851.2:c.*231A= NP_062825.1:n.*231A=
NM_019851.3:c.*231A= MANE Select NP_062825.1:n.*231A=
Search 100 bp 5'
Search 100 bp 3'