Canonical Allele Identifier: CA1160468898

Gene: FCN3

Linked Data

• dbSNP Id: rs3813800
• gnomAD v4: 1-27370983-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.27370983G>A , CM000663.2:g.27370983G>A	GRCh38
NC_000001.10:g.27697474G>A , CM000663.1:g.27697474G>A	GRCh37
NC_000001.9:g.27570061G>A	NCBI36
NG_016279.1:g.8842C>T , LRG_171:g.8842C>T
NG_051309.1:g.2055C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000699962.1:n.393-11C>T
ENST00000699963.1:c.394-11C>T	ENSP00000514719.1:n.394-11C>T
ENST00000270879.9:c.394-11C>T MANE Select	ENSP00000270879.4:n.394-11C>T
ENST00000270879.8:c.394-11C>T	ENSP00000270879.4:n.394-11C>T
ENST00000354982.2:c.361-11C>T	ENSP00000347077.2:n.361-11C>T
ENST00000498393.1:n.544-11C>T
NM_003665.2:c.394-11C>T , LRG_171t1:c.394-11C>T	NP_003656.2:n.394-11C>T
NM_173452.1:c.361-11C>T	NP_775628.1:n.361-11C>T
XM_011542339.1:c.394-11C>T	XP_011540641.1:n.394-11C>T
NM_003665.3:c.394-11C>T	NP_003656.2:n.394-11C>T
NM_173452.2:c.361-11C>T	NP_775628.1:n.361-11C>T
NM_003665.4:c.394-11C>T MANE Select	NP_003656.2:n.394-11C>T
NM_173452.3:c.361-11C>T	NP_775628.1:n.361-11C>T