Canonical Allele Identifier: CA2686252316
Gene: FGF20 HGNC NCBI

Linked Data

gnomAD v4: 8-16992797-T-C

Genomic Alleles

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

Transcript Alleles

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