Canonical Allele Identifier: CA529000588

Gene: IRF6

Linked Data

• dbSNP Id: rs1404291807
• gnomAD v2: 1-209974764-G-A
• gnomAD v4: 1-209801419-G-A
• MyVariant Identifiers: chr1:g.209974764G>A (hg19) ; chr1:g.209801419G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209801419G>A , CM000663.2:g.209801419G>A	GRCh38
NC_000001.10:g.209974764G>A , CM000663.1:g.209974764G>A	GRCh37
NC_000001.9:g.208041387G>A	NCBI36
NG_007081.2:g.9716C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696133.1:c.-3-3C>T	ENSP00000512426.1:n.-3-3C>T
ENST00000696134.1:c.-3-3C>T	ENSP00000512427.1:n.-3-3C>T
ENST00000367021.8:c.-3-3C>T MANE Select	ENSP00000355988.3:n.-3-3C>T
ENST00000643798.1:c.-3-3C>T	ENSP00000496669.1:n.-3-3C>T
ENST00000367021.7:c.-3-3C>T	ENSP00000355988.3:n.-3-3C>T
ENST00000456314.1:c.-3-3C>T	ENSP00000403855.1:n.-3-3C>T
ENST00000542854.5:c.-112+4528C>T	ENSP00000440532.1:n.-112+4528C>T
NM_001206696.1:c.-112+4528C>T	NP_001193625.1:n.-112+4528C>T
NM_006147.3:c.-3-3C>T	NP_006138.1:n.-3-3C>T
NM_006147.4:c.-3-3C>T MANE Select	NP_006138.1:n.-3-3C>T
NM_001206696.2:c.-112+4528C>T	NP_001193625.1:n.-112+4528C>T