Canonical Allele Identifier: CA381664539
Gene: FGF3 HGNC NCBI

Linked Data

gnomAD v4: 11-69818815-C-A
MyVariant Identifiers: chr11:g.69633583C>A (hg19) chr11:g.69818815C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69818815C>A , CM000673.2:g.69818815C>A GRCh38
NC_000011.9:g.69633583C>A , CM000673.1:g.69633583C>A GRCh37
NC_000011.8:g.69342520C>A NCBI36
NG_009016.1:g.5610G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000334134.4:c.119G>T MANE Select ENSP00000334122.2:p.Gly40Val
ENST00000334134.2:c.119G>T ENSP00000334122.2:p.Gly40Val
NM_005247.2:c.119G>T NP_005238.1:p.Gly40Val
NM_005247.3:c.119G>T NP_005238.1:p.Gly40Val
NM_005247.4:c.119G>T MANE Select NP_005238.1:p.Gly40Val
Search 100 bp 5'
Search 100 bp 3'