Canonical Allele Identifier: CA1011779998
Gene: IRF6 HGNC NCBI

Linked Data

gnomAD v3: 1-209801216-C-T
gnomAD v4: 1-209801216-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209801216C>T , CM000663.2:g.209801216C>T GRCh38
NC_000001.10:g.209974561C>T , CM000663.1:g.209974561C>T GRCh37
NC_000001.9:g.208041184C>T NCBI36
NG_007081.2:g.9919G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000696133.1:c.174+24G>A ENSP00000512426.1:n.174+24G>A
ENST00000696134.1:c.174+24G>A ENSP00000512427.1:n.174+24G>A
ENST00000367021.8:c.174+24G>A MANE Select ENSP00000355988.3:n.174+24G>A
ENST00000643798.1:c.174+24G>A ENSP00000496669.1:n.174+24G>A
ENST00000367021.7:c.174+24G>A ENSP00000355988.3:n.174+24G>A
ENST00000456314.1:c.174+24G>A ENSP00000403855.1:n.174+24G>A
ENST00000542854.5:c.-111-4664G>A ENSP00000440532.1:n.-111-4664G>A
NM_001206696.1:c.-111-4664G>A NP_001193625.1:n.-111-4664G>A
NM_006147.3:c.174+24G>A NP_006138.1:n.174+24G>A
NM_006147.4:c.174+24G>A MANE Select NP_006138.1:n.174+24G>A
NM_001206696.2:c.-111-4664G>A NP_001193625.1:n.-111-4664G>A
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