Canonical Allele Identifier: CA16609477
Gene: IRF6 HGNC NCBI

Linked Data

ClinVar Variation Id: 397639
ClinVar RCV Id: RCV000449637
dbSNP Id: rs1060499555

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209801301A>G , CM000663.2:g.209801301A>G GRCh38
NC_000001.10:g.209974646A>G , CM000663.1:g.209974646A>G GRCh37
NC_000001.9:g.208041269A>G NCBI36
NG_007081.2:g.9834T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000696133.1:c.113T>C ENSP00000512426.1:p.Ile38Thr
ENST00000696134.1:c.113T>C ENSP00000512427.1:p.Ile38Thr
ENST00000367021.8:c.113T>C MANE Select ENSP00000355988.3:p.Ile38Thr
ENST00000643798.1:c.113T>C ENSP00000496669.1:p.Ile38Thr
ENST00000367021.7:c.113T>C ENSP00000355988.3:p.Ile38Thr
ENST00000456314.1:c.113T>C ENSP00000403855.1:p.Ile38Thr
ENST00000542854.5:c.-112+4646T>C ENSP00000440532.1:n.-112+4646T>C
NM_001206696.1:c.-112+4646T>C NP_001193625.1:n.-112+4646T>C
NM_006147.3:c.113T>C NP_006138.1:p.Ile38Thr
NM_006147.4:c.113T>C MANE Select NP_006138.1:p.Ile38Thr
NM_001206696.2:c.-112+4646T>C NP_001193625.1:n.-112+4646T>C