Canonical Allele Identifier: CA528646041

Gene: IRF6

Linked Data

• dbSNP Id: rs1488622761
• gnomAD v2: 1-209968589-C-T
• MyVariant Identifiers: chr1:g.209968589C>T (hg19) ; chr1:g.209795244C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209795244C>T , CM000663.2:g.209795244C>T	GRCh38
NC_000001.10:g.209968589C>T , CM000663.1:g.209968589C>T	GRCh37
NC_000001.9:g.208035212C>T	NCBI36
NG_007081.2:g.15891G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696133.1:c.508+46G>A	ENSP00000512426.1:n.508+46G>A
ENST00000696134.1:c.508+46G>A	ENSP00000512427.1:n.508+46G>A
ENST00000367021.8:c.508+46G>A MANE Select	ENSP00000355988.3:n.508+46G>A
ENST00000643798.1:c.508+46G>A	ENSP00000496669.1:n.508+46G>A
ENST00000367021.7:c.508+46G>A	ENSP00000355988.3:n.508+46G>A
ENST00000456314.1:c.508+46G>A	ENSP00000403855.1:n.508+46G>A
ENST00000542854.5:c.223+46G>A	ENSP00000440532.1:n.223+46G>A
NM_001206696.1:c.223+46G>A	NP_001193625.1:n.223+46G>A
NM_006147.3:c.508+46G>A	NP_006138.1:n.508+46G>A
NM_006147.4:c.508+46G>A MANE Select	NP_006138.1:n.508+46G>A
NM_001206696.2:c.223+46G>A	NP_001193625.1:n.223+46G>A