Canonical Allele Identifier: CA13668005
Gene: NFE2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10506328

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.54293448A>C , CM000674.2:g.54293448A>C GRCh38
NC_000012.11:g.54687232A>C , CM000674.1:g.54687232A>C GRCh37
NC_000012.10:g.52973499A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001136023.2:c.115-67T>G VV NP_001129495.1:p.=
NM_001261461.1:c.115-67T>G VV NP_001248390.1:p.=
NM_006163.2:c.115-67T>G VV NP_006154.1:p.=
XM_005268906.3:c.115-67T>G XP_005268963.1:p.=
XM_011538397.1:c.82-67T>G XP_011536699.1:p.=
XM_005268906.4:c.115-67T>G
NM_001136023.3:c.115-67T>G VV MANE Preferred
ENST00000312156.8:c.115-67T>G ENSP00000312436.4:p.=
ENST00000435572.6:c.115-67T>G ENSP00000397185.2:p.=
ENST00000540264.2:c.115-67T>G ENSP00000439120.2:p.=
ENST00000553070.5:c.115-67T>G ENSP00000447558.1:p.=
ENST00000553198.1:c.115-67T>G ENSP00000446929.1:p.=