Canonical Allele Identifier: CA2484364096
Gene: IRF6 HGNC NCBI

Linked Data

dbSNP Id: rs1571976986

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209786268G>A , CM000663.2:g.209786268G>A GRCh38
NC_000001.10:g.209959613G>A , CM000663.1:g.209959613G>A GRCh37
NC_000001.9:g.208026236G>A NCBI36
NG_007081.2:g.24867C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696133.1:c.1400+2156C>T ENSP00000512426.1:n.1400+2156C>T
ENST00000696134.1:c.*2983C>T ENSP00000512427.1:n.*2983C>T
ENST00000367021.8:c.*2152C>T MANE Select ENSP00000355988.3:n.*2152C>T
ENST00000367021.7:c.*2152C>T ENSP00000355988.3:n.*2152C>T
ENST00000542854.5:c.*2152C>T ENSP00000440532.1:n.*2152C>T
NM_001206696.1:c.*2152C>T NP_001193625.1:n.*2152C>T
NM_006147.3:c.*2152C>T NP_006138.1:n.*2152C>T
NM_006147.4:c.*2152C>T MANE Select NP_006138.1:n.*2152C>T
NM_001206696.2:c.*2152C>T NP_001193625.1:n.*2152C>T