Canonical Allele Identifier: CA381664534
Gene: FGF3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.69633580C>G (hg19) chr11:g.69818812C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69818812C>G , CM000673.2:g.69818812C>G GRCh38
NC_000011.9:g.69633580C>G , CM000673.1:g.69633580C>G GRCh37
NC_000011.8:g.69342517C>G NCBI36
NG_009016.1:g.5613G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000334134.4:c.122G>C MANE Select ENSP00000334122.2:p.Gly41Ala
ENST00000334134.2:c.122G>C ENSP00000334122.2:p.Gly41Ala
NM_005247.2:c.122G>C NP_005238.1:p.Gly41Ala
NM_005247.3:c.122G>C NP_005238.1:p.Gly41Ala
NM_005247.4:c.122G>C MANE Select NP_005238.1:p.Gly41Ala
Search 100 bp 5'
Search 100 bp 3'