Canonical Allele Identifier: CA381664459
Gene: FGF3 HGNC NCBI

Linked Data

gnomAD v4: 11-69818776-T-A
MyVariant Identifiers: chr11:g.69633544T>A (hg19) chr11:g.69818776T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69818776T>A , CM000673.2:g.69818776T>A GRCh38
NC_000011.9:g.69633544T>A , CM000673.1:g.69633544T>A GRCh37
NC_000011.8:g.69342481T>A NCBI36
NG_009016.1:g.5649A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000334134.4:c.158A>T MANE Select ENSP00000334122.2:p.Lys53Met
ENST00000334134.2:c.158A>T ENSP00000334122.2:p.Lys53Met
NM_005247.2:c.158A>T NP_005238.1:p.Lys53Met
NM_005247.3:c.158A>T NP_005238.1:p.Lys53Met
NM_005247.4:c.158A>T MANE Select NP_005238.1:p.Lys53Met
Search 100 bp 5'
Search 100 bp 3'