Canonical Allele Identifier: CA475468077

Gene: FGF3

Linked Data

• MyVariant Identifiers: chr11:g.69625295G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69810527G>T , CM000673.2:g.69810527G>T	GRCh38
NC_000011.9:g.69625295G>T , CM000673.1:g.69625295G>T	GRCh37
NC_000011.8:g.69334476G>T	NCBI36
NG_009016.1:g.13898C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334134.4:c.498C>A MANE Select	ENSP00000334122.2:p.Gly166=
ENST00000646078.1:n.345C>A
ENST00000334134.2:c.498C>A	ENSP00000334122.2:p.Gly166=
NM_005247.2:c.498C>A	NP_005238.1:p.Gly166=
NM_005247.3:c.498C>A	NP_005238.1:p.Gly166=
NM_005247.4:c.498C>A MANE Select	NP_005238.1:p.Gly166=