Canonical Allele Identifier: CA1377325
Gene: IRF6 HGNC NCBI

Linked Data

dbSNP Id: rs2013162

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209795339C>T , CM000663.2:g.209795339C>T GRCh38
NC_000001.10:g.209968684C>T , CM000663.1:g.209968684C>T GRCh37
NC_000001.9:g.208035307C>T NCBI36
NG_007081.2:g.15796G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000696133.1:c.459G>A ENSP00000512426.1:p.Ser153=
ENST00000696134.1:c.459G>A ENSP00000512427.1:p.Ser153=
ENST00000367021.8:c.459G>A MANE Select ENSP00000355988.3:p.Ser153=
ENST00000643798.1:c.459G>A ENSP00000496669.1:p.Ser153=
ENST00000367021.7:c.459G>A ENSP00000355988.3:p.Ser153=
ENST00000456314.1:c.459G>A ENSP00000403855.1:p.Ser153=
ENST00000542854.5:c.174G>A ENSP00000440532.1:p.Ser58=
NM_001206696.1:c.174G>A NP_001193625.1:p.Ser58=
NM_006147.3:c.459G>A NP_006138.1:p.Ser153=
NM_006147.4:c.459G>A MANE Select NP_006138.1:p.Ser153=
NM_001206696.2:c.174G>A NP_001193625.1:p.Ser58=