Canonical Allele Identifier: CA714242

Gene: FCN3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.27370658C>T , CM000663.2:g.27370658C>T	GRCh38
NC_000001.10:g.27697149C>T , CM000663.1:g.27697149C>T	GRCh37
NC_000001.9:g.27569736C>T	NCBI36
NG_016279.1:g.9167G>A , LRG_171:g.9167G>A
NG_051309.1:g.2380G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699962.1:n.595G>A
ENST00000699963.1:c.596G>A	ENSP00000514719.1:p.Arg199His
ENST00000270879.9:c.596G>A MANE Select	ENSP00000270879.4:p.Arg199His
ENST00000270879.8:c.596G>A	ENSP00000270879.4:p.Arg199His
ENST00000354982.2:c.563G>A	ENSP00000347077.2:p.Arg188His
ENST00000498393.1:n.746G>A
NM_003665.2:c.596G>A , LRG_171t1:c.596G>A	NP_003656.2:p.Arg199His
NM_173452.1:c.563G>A	NP_775628.1:p.Arg188His
XM_011542339.1:c.596G>A	XP_011540641.1:p.Arg199His
NM_003665.3:c.596G>A	NP_003656.2:p.Arg199His
NM_173452.2:c.563G>A	NP_775628.1:p.Arg188His
NM_003665.4:c.596G>A MANE Select	NP_003656.2:p.Arg199His
NM_173452.3:c.563G>A	NP_775628.1:p.Arg188His