Canonical Allele Identifier: CA1377404

Gene: IRF6

Linked Data

• dbSNP Id: rs758936784
• ExAC: 1:209974679 A / C
• gnomAD v2: 1-209974679-A-C
• gnomAD v4: 1-209801334-A-C
• MyVariant Identifiers: chr1:g.209974679A>C (hg19) ; chr1:g.209801334A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209801334A>C , CM000663.2:g.209801334A>C	GRCh38
NC_000001.10:g.209974679A>C , CM000663.1:g.209974679A>C	GRCh37
NC_000001.9:g.208041302A>C	NCBI36
NG_007081.2:g.9801T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696133.1:c.80T>G	ENSP00000512426.1:p.Ile27Ser
ENST00000696134.1:c.80T>G	ENSP00000512427.1:p.Ile27Ser
ENST00000367021.8:c.80T>G MANE Select	ENSP00000355988.3:p.Ile27Ser
ENST00000643798.1:c.80T>G	ENSP00000496669.1:p.Ile27Ser
ENST00000367021.7:c.80T>G	ENSP00000355988.3:p.Ile27Ser
ENST00000456314.1:c.80T>G	ENSP00000403855.1:p.Ile27Ser
ENST00000542854.5:c.-112+4613T>G	ENSP00000440532.1:n.-112+4613T>G
NM_001206696.1:c.-112+4613T>G	NP_001193625.1:n.-112+4613T>G
NM_006147.3:c.80T>G	NP_006138.1:p.Ile27Ser
NM_006147.4:c.80T>G MANE Select	NP_006138.1:p.Ile27Ser
NM_001206696.2:c.-112+4613T>G	NP_001193625.1:n.-112+4613T>G