Canonical Allele Identifier: CA381663712
Gene: FGF3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.69625294A>C (hg19) chr11:g.69810526A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69810526A>C , CM000673.2:g.69810526A>C GRCh38
NC_000011.9:g.69625294A>C , CM000673.1:g.69625294A>C GRCh37
NC_000011.8:g.69334475A>C NCBI36
NG_009016.1:g.13899T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000334134.4:c.499T>G MANE Select ENSP00000334122.2:p.Phe167Val
ENST00000646078.1:n.346T>G
ENST00000334134.2:c.499T>G ENSP00000334122.2:p.Phe167Val
NM_005247.2:c.499T>G NP_005238.1:p.Phe167Val
NM_005247.3:c.499T>G NP_005238.1:p.Phe167Val
NM_005247.4:c.499T>G MANE Select NP_005238.1:p.Phe167Val
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