Canonical Allele Identifier: CA2686252461
Gene: FGF20 HGNC NCBI

Linked Data

gnomAD v4: 8-16992947-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992947C>T , CM000670.2:g.16992947C>T GRCh38
NC_000008.10:g.16850456C>T , CM000670.1:g.16850456C>T GRCh37
NC_000008.9:g.16894827C>T NCBI36
NG_015978.1:g.14219G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*125G>A MANE Select ENSP00000180166.5:n.*125G>A
ENST00000180166.5:c.*125G>A ENSP00000180166.5:n.*125G>A
NM_019851.2:c.*125G>A NP_062825.1:n.*125G>A
NM_019851.3:c.*125G>A MANE Select NP_062825.1:n.*125G>A
Search 100 bp 5'
Search 100 bp 3'