Canonical Allele Identifier: CA2686252333
Gene: FGF20 HGNC NCBI

Linked Data

gnomAD v4: 8-16992818-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992818G>T , CM000670.2:g.16992818G>T GRCh38
NC_000008.10:g.16850327G>T , CM000670.1:g.16850327G>T GRCh37
NC_000008.9:g.16894698G>T NCBI36
NG_015978.1:g.14348C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000180166.6:c.*254C>A MANE Select ENSP00000180166.5:n.*254C>A
ENST00000180166.5:c.*254C>A ENSP00000180166.5:n.*254C>A
NM_019851.3:c.*254C>A MANE Select NP_062825.1:n.*254C>A