Canonical Allele Identifier: CA2686252183
Gene: FGF20 HGNC NCBI

Linked Data

gnomAD v4: 8-16992614-T-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992614T>G , CM000670.2:g.16992614T>G GRCh38
NC_000008.10:g.16850123T>G , CM000670.1:g.16850123T>G GRCh37
NC_000008.9:g.16894494T>G NCBI36
NG_015978.1:g.14552A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*458A>C MANE Select ENSP00000180166.5:n.*458A>C
ENST00000180166.5:c.*458A>C ENSP00000180166.5:n.*458A>C
NM_019851.3:c.*458A>C MANE Select NP_062825.1:n.*458A>C
Search 100 bp 5'
Search 100 bp 3'