Canonical Allele Identifier: CA2484364041
Gene: IRF6 HGNC NCBI

Linked Data

dbSNP Id: rs2077832161

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209786146A>C , CM000663.2:g.209786146A>C GRCh38
NC_000001.10:g.209959491A>C , CM000663.1:g.209959491A>C GRCh37
NC_000001.9:g.208026114A>C NCBI36
NG_007081.2:g.24989T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696133.1:c.1400+2278T>G ENSP00000512426.1:n.1400+2278T>G
ENST00000696134.1:c.*3105T>G ENSP00000512427.1:n.*3105T>G
ENST00000367021.8:c.*2274T>G MANE Select ENSP00000355988.3:n.*2274T>G
ENST00000367021.7:c.*2274T>G ENSP00000355988.3:n.*2274T>G
ENST00000542854.5:c.*2274T>G ENSP00000440532.1:n.*2274T>G
NM_001206696.1:c.*2274T>G NP_001193625.1:n.*2274T>G
NM_006147.3:c.*2274T>G NP_006138.1:n.*2274T>G
NM_006147.4:c.*2274T>G MANE Select NP_006138.1:n.*2274T>G
NM_001206696.2:c.*2274T>G NP_001193625.1:n.*2274T>G