Canonical Allele Identifier: CA1111331268
Gene: FGF20 HGNC NCBI

Linked Data

dbSNP Id: rs968892541
gnomAD v3: 8-16992424-G-T
gnomAD v4: 8-16992424-G-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992424G>T , CM000670.2:g.16992424G>T GRCh38
NC_000008.10:g.16849933G>T , CM000670.1:g.16849933G>T GRCh37
NC_000008.9:g.16894304G>T NCBI36
NG_015978.1:g.14742C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*648C>A MANE Select ENSP00000180166.5:n.*648C>A
ENST00000180166.5:c.*648C>A ENSP00000180166.5:n.*648C>A
NM_019851.3:c.*648C>A MANE Select NP_062825.1:n.*648C>A
Search 100 bp 5'
Search 100 bp 3'