Canonical Allele Identifier: CA2686252399
Gene: FGF20 HGNC NCBI

Linked Data

gnomAD v4: 8-16992897-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992897T>A , CM000670.2:g.16992897T>A GRCh38
NC_000008.10:g.16850406T>A , CM000670.1:g.16850406T>A GRCh37
NC_000008.9:g.16894777T>A NCBI36
NG_015978.1:g.14269A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000180166.6:c.*175A>T MANE Select ENSP00000180166.5:n.*175A>T
ENST00000180166.5:c.*175A>T ENSP00000180166.5:n.*175A>T
NM_019851.2:c.*175A>T NP_062825.1:n.*175A>T
NM_019851.3:c.*175A>T MANE Select NP_062825.1:n.*175A>T