Canonical Allele Identifier: CA36754572

Gene: IRF6

Linked Data

• dbSNP Id: rs942367975
• gnomAD v3: 1-209795506-T-C
• gnomAD v4: 1-209795506-T-C
• MyVariant Identifiers: chr1:g.209968851T>C (hg19) ; chr1:g.209795506T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209795506T>C , CM000663.2:g.209795506T>C	GRCh38
NC_000001.10:g.209968851T>C , CM000663.1:g.209968851T>C	GRCh37
NC_000001.9:g.208035474T>C	NCBI36
NG_007081.2:g.15629A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696133.1:c.380-88A>G	ENSP00000512426.1:n.380-88A>G
ENST00000696134.1:c.380-88A>G	ENSP00000512427.1:n.380-88A>G
ENST00000367021.8:c.380-88A>G MANE Select	ENSP00000355988.3:n.380-88A>G
ENST00000643798.1:c.380-88A>G	ENSP00000496669.1:n.380-88A>G
ENST00000367021.7:c.380-88A>G	ENSP00000355988.3:n.380-88A>G
ENST00000456314.1:c.380-88A>G	ENSP00000403855.1:n.380-88A>G
ENST00000542854.5:c.95-88A>G	ENSP00000440532.1:n.95-88A>G
NM_001206696.1:c.95-88A>G	NP_001193625.1:n.95-88A>G
NM_006147.3:c.380-88A>G	NP_006138.1:n.380-88A>G
NM_006147.4:c.380-88A>G MANE Select	NP_006138.1:n.380-88A>G
NM_001206696.2:c.95-88A>G	NP_001193625.1:n.95-88A>G