Canonical Allele Identifier: CA2484364097
Gene: IRF6 HGNC NCBI

Linked Data

dbSNP Id: rs1044516

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209786269G>C , CM000663.2:g.209786269G>C GRCh38
NC_000001.10:g.209959614G>C , CM000663.1:g.209959614G>C GRCh37
NC_000001.9:g.208026237G>C NCBI36
NG_007081.2:g.24866C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000696133.1:c.1400+2155C>G ENSP00000512426.1:n.1400+2155C>G
ENST00000696134.1:c.*2982C>G ENSP00000512427.1:n.*2982C>G
ENST00000367021.8:c.*2151C>G MANE Select ENSP00000355988.3:n.*2151C>G
ENST00000367021.7:c.*2151C>G ENSP00000355988.3:n.*2151C>G
ENST00000542854.5:c.*2151C>G ENSP00000440532.1:n.*2151C>G
NM_001206696.1:c.*2151C>G NP_001193625.1:n.*2151C>G
NM_006147.3:c.*2151C>G NP_006138.1:n.*2151C>G
NM_006147.4:c.*2151C>G MANE Select NP_006138.1:n.*2151C>G
NM_001206696.2:c.*2151C>G NP_001193625.1:n.*2151C>G