Canonical Allele Identifier: CA2484363898
Gene: IRF6 HGNC NCBI

Linked Data

dbSNP Id: rs2077830864

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209785959C>G , CM000663.2:g.209785959C>G GRCh38
NC_000001.10:g.209959304C>G , CM000663.1:g.209959304C>G GRCh37
NC_000001.9:g.208025927C>G NCBI36
NG_007081.2:g.25176G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000696133.1:c.1401-2250G>C ENSP00000512426.1:n.1401-2250G>C
ENST00000696134.1:c.*3292G>C ENSP00000512427.1:n.*3292G>C
ENST00000367021.8:c.*2461G>C MANE Select ENSP00000355988.3:n.*2461G>C
ENST00000367021.7:c.*2461G>C ENSP00000355988.3:n.*2461G>C
ENST00000542854.5:c.*2461G>C ENSP00000440532.1:n.*2461G>C
NM_001206696.1:c.*2461G>C NP_001193625.1:n.*2461G>C
NM_006147.3:c.*2461G>C NP_006138.1:n.*2461G>C
NM_006147.4:c.*2461G>C MANE Select NP_006138.1:n.*2461G>C
NM_001206696.2:c.*2461G>C NP_001193625.1:n.*2461G>C