Canonical Allele Identifier: CA2484367118

Gene: IRF6

Linked Data

• dbSNP Id: rs2077892194

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209795051G>T , CM000663.2:g.209795051G>T	GRCh38
NC_000001.10:g.209968396G>T , CM000663.1:g.209968396G>T	GRCh37
NC_000001.9:g.208035019G>T	NCBI36
NG_007081.2:g.16084C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696133.1:c.508+239C>A	ENSP00000512426.1:n.508+239C>A
ENST00000696134.1:c.508+239C>A	ENSP00000512427.1:n.508+239C>A
ENST00000367021.8:c.508+239C>A MANE Select	ENSP00000355988.3:n.508+239C>A
ENST00000643798.1:c.508+239C>A	ENSP00000496669.1:n.508+239C>A
ENST00000367021.7:c.508+239C>A	ENSP00000355988.3:n.508+239C>A
ENST00000456314.1:c.508+239C>A	ENSP00000403855.1:n.508+239C>A
ENST00000542854.5:c.223+239C>A	ENSP00000440532.1:n.223+239C>A
NM_001206696.1:c.223+239C>A	NP_001193625.1:n.223+239C>A
NM_006147.3:c.508+239C>A	NP_006138.1:n.508+239C>A
NM_006147.4:c.508+239C>A MANE Select	NP_006138.1:n.508+239C>A
NM_001206696.2:c.223+239C>A	NP_001193625.1:n.223+239C>A