Canonical Allele Identifier: CA2686252315
Gene: FGF20 HGNC NCBI

Linked Data

gnomAD v4: 8-16992797-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992797T>A , CM000670.2:g.16992797T>A GRCh38
NC_000008.10:g.16850306T>A , CM000670.1:g.16850306T>A GRCh37
NC_000008.9:g.16894677T>A NCBI36
NG_015978.1:g.14369A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000180166.6:c.*275A>T MANE Select ENSP00000180166.5:n.*275A>T
ENST00000180166.5:c.*275A>T ENSP00000180166.5:n.*275A>T
NM_019851.3:c.*275A>T MANE Select NP_062825.1:n.*275A>T