Canonical Allele Identifier: CA381663655
Gene: FGF3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.69625266G>C (hg19) chr11:g.69810498G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69810498G>C , CM000673.2:g.69810498G>C GRCh38
NC_000011.9:g.69625266G>C , CM000673.1:g.69625266G>C GRCh37
NC_000011.8:g.69334447G>C NCBI36
NG_009016.1:g.13927C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000334134.4:c.527C>G MANE Select ENSP00000334122.2:p.Ser176Cys
ENST00000646078.1:n.374C>G
ENST00000334134.2:c.527C>G ENSP00000334122.2:p.Ser176Cys
NM_005247.2:c.527C>G NP_005238.1:p.Ser176Cys
NM_005247.3:c.527C>G NP_005238.1:p.Ser176Cys
NM_005247.4:c.527C>G MANE Select NP_005238.1:p.Ser176Cys
Search 100 bp 5'
Search 100 bp 3'