Canonical Allele Identifier: CA475221997
Gene: FGF3 HGNC NCBI

Linked Data

gnomAD v4: 11-69818736-G-C
MyVariant Identifiers: chr11:g.69633504G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69818736G>C , CM000673.2:g.69818736G>C GRCh38
NC_000011.9:g.69633504G>C , CM000673.1:g.69633504G>C GRCh37
NC_000011.8:g.69342441G>C NCBI36
NG_009016.1:g.5689C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000334134.4:c.198C>G MANE Select ENSP00000334122.2:p.Gly66=
ENST00000334134.2:c.198C>G ENSP00000334122.2:p.Gly66=
NM_005247.2:c.198C>G NP_005238.1:p.Gly66=
NM_005247.3:c.198C>G NP_005238.1:p.Gly66=
NM_005247.4:c.198C>G MANE Select NP_005238.1:p.Gly66=
Search 100 bp 5'
Search 100 bp 3'