Canonical Allele Identifier: CA714311

Gene: FCN3

Linked Data

• dbSNP Id: rs3813800
• ExAC: 1:27697474 G / T
• gnomAD v2: 1-27697474-G-T
• gnomAD v3: 1-27370983-G-T
• gnomAD v4: 1-27370983-G-T
• MyVariant Identifiers: chr1:g.27697474G>T (hg19) ; chr1:g.27370983G>T (hg38)

Genomic Alleles

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

Transcript Alleles

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