Canonical Allele Identifier: CA1767395669
Gene: FGF20 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992827C= , CM000670.2:g.16992827C= GRCh38
NC_000008.10:g.16850336C= , CM000670.1:g.16850336C= GRCh37
NC_000008.9:g.16894707C= NCBI36
NG_015978.1:g.14339G=

Transcript Alleles

HGVS Amino-acid change
ENST00000180166.6:c.*245G= MANE Select ENSP00000180166.5:n.*245G=
ENST00000180166.5:c.*245G= ENSP00000180166.5:n.*245G=
NM_019851.2:c.*245G= NP_062825.1:n.*245G=
NM_019851.3:c.*245G= MANE Select NP_062825.1:n.*245G=