Canonical Allele Identifier: CA11167716
Gene: NFE2L2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs6726395

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.177238501A>G , CM000664.2:g.177238501A>G GRCh38
NC_000002.11:g.178103229A>G , CM000664.1:g.178103229A>G GRCh37
NC_000002.10:g.177811475A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001145412.2:c.-3-4230T>C VV NP_001138884.1:p.=
NM_001145412.3:c.-3-4230T>C VV NP_001138884.1:p.=
NM_001145413.2:c.-3-4230T>C VV NP_001138885.1:p.=
NM_001145413.3:c.-3-4230T>C VV NP_001138885.1:p.=
NM_001313900.1:c.-3-4230T>C VV NP_001300829.1:p.=
NM_001313901.1:c.-3-4230T>C VV NP_001300830.1:p.=
NM_001313902.1:c.46-4230T>C VV NP_001300831.1:p.=
NM_001313903.1:c.46-4230T>C VV NP_001300832.1:p.=
NM_001313904.1:c.-184-4230T>C VV NP_001300833.1:p.=
NM_006164.4:c.46-4230T>C VV NP_006155.2:p.=
NM_006164.5:c.46-4230T>C VV NP_006155.2:p.=
ENST00000397062.7:c.46-4230T>C ENSP00000380252.3:p.=
ENST00000397063.8:c.-3-4230T>C ENSP00000380253.4:p.=
ENST00000421929.5:c.-3-4230T>C ENSP00000412191.1:p.=
ENST00000423513.5:c.-3-4230T>C ENSP00000410015.1:p.=
ENST00000430047.1:c.46-4230T>C ENSP00000391291.1:p.=
ENST00000446151.6:c.-3-4230T>C ENSP00000411575.2:p.=
ENST00000448782.5:c.-3-4230T>C ENSP00000400073.1:p.=
ENST00000449627.1:c.-3-4230T>C ENSP00000391590.1:p.=
ENST00000462023.1:n.129-4230T>C
ENST00000464747.5:c.-3-4230T>C ENSP00000467401.1:p.=
ENST00000477534.1:n.136-4230T>C
ENST00000586532.5:c.43-4230T>C ENSP00000464920.1:p.=
ENST00000588123.1:c.-3-4230T>C ENSP00000468089.1:p.=