Canonical Allele Identifier: CA381663630
Gene: FGF3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.69625252G>C (hg19) chr11:g.69810484G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69810484G>C , CM000673.2:g.69810484G>C GRCh38
NC_000011.9:g.69625252G>C , CM000673.1:g.69625252G>C GRCh37
NC_000011.8:g.69334433G>C NCBI36
NG_009016.1:g.13941C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000334134.4:c.541C>G MANE Select ENSP00000334122.2:p.Arg181Gly
ENST00000646078.1:n.388C>G
ENST00000334134.2:c.541C>G ENSP00000334122.2:p.Arg181Gly
NM_005247.2:c.541C>G NP_005238.1:p.Arg181Gly
NM_005247.3:c.541C>G NP_005238.1:p.Arg181Gly
NM_005247.4:c.541C>G MANE Select NP_005238.1:p.Arg181Gly
Search 100 bp 5'
Search 100 bp 3'