Canonical Allele Identifier: CA381663757

Gene: FGF3

Linked Data

• MyVariant Identifiers: chr11:g.69625317C>A (hg19) ; chr11:g.69810549C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69810549C>A , CM000673.2:g.69810549C>A	GRCh38
NC_000011.9:g.69625317C>A , CM000673.1:g.69625317C>A	GRCh37
NC_000011.8:g.69334498C>A	NCBI36
NG_009016.1:g.13876G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334134.4:c.476G>T MANE Select	ENSP00000334122.2:p.Gly159Val
ENST00000646078.1:n.323G>T
ENST00000334134.2:c.476G>T	ENSP00000334122.2:p.Gly159Val
NM_005247.2:c.476G>T	NP_005238.1:p.Gly159Val
NM_005247.3:c.476G>T	NP_005238.1:p.Gly159Val
NM_005247.4:c.476G>T MANE Select	NP_005238.1:p.Gly159Val