Canonical Allele Identifier: CA475222224
Gene: FGF3 HGNC NCBI

Linked Data

gnomAD v4: 11-69818823-C-T
MyVariant Identifiers: chr11:g.69633591C>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69818823C>T , CM000673.2:g.69818823C>T GRCh38
NC_000011.9:g.69633591C>T , CM000673.1:g.69633591C>T GRCh37
NC_000011.8:g.69342528C>T NCBI36
NG_009016.1:g.5602G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000334134.4:c.111G>A MANE Select ENSP00000334122.2:p.Glu37=
ENST00000334134.2:c.111G>A ENSP00000334122.2:p.Glu37=
NM_005247.2:c.111G>A NP_005238.1:p.Glu37=
NM_005247.3:c.111G>A NP_005238.1:p.Glu37=
NM_005247.4:c.111G>A MANE Select NP_005238.1:p.Glu37=
Search 100 bp 5'
Search 100 bp 3'