Canonical Allele Identifier: CA2614802140
Gene: FGF3 HGNC NCBI

Linked Data

gnomAD v4: 11-69818754-CG-C
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69818757del , CM000673.2:g.69818757del GRCh38
NC_000011.9:g.69633525del , CM000673.1:g.69633525del GRCh37
NC_000011.8:g.69342462del NCBI36
NG_009016.1:g.5670del

Transcript Alleles

HGVS Amino-acid Change
ENST00000334134.4:c.179del MANE Select ENSP00000334122.2:p.Pro60ArgfsTer19
ENST00000334134.2:c.179del ENSP00000334122.2:p.Pro60ArgfsTer19
NM_005247.2:c.179del NP_005238.1:p.Pro60ArgfsTer19
NM_005247.3:c.179del NP_005238.1:p.Pro60ArgfsTer19
NM_005247.4:c.179del MANE Select NP_005238.1:p.Pro60ArgfsTer19
Search 100 bp 5'
Search 100 bp 3'