Canonical Allele Identifier: CA381663769
Gene: FGF3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.69625321T>G (hg19) chr11:g.69810553T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69810553T>G , CM000673.2:g.69810553T>G GRCh38
NC_000011.9:g.69625321T>G , CM000673.1:g.69625321T>G GRCh37
NC_000011.8:g.69334502T>G NCBI36
NG_009016.1:g.13872A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000334134.4:c.472A>C MANE Select ENSP00000334122.2:p.Asn158His
ENST00000646078.1:n.319A>C
ENST00000334134.2:c.472A>C ENSP00000334122.2:p.Asn158His
NM_005247.2:c.472A>C NP_005238.1:p.Asn158His
NM_005247.3:c.472A>C NP_005238.1:p.Asn158His
NM_005247.4:c.472A>C MANE Select NP_005238.1:p.Asn158His
Search 100 bp 5'
Search 100 bp 3'