Canonical Allele Identifier: CA2336178802
Gene: CYP2A6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40848286T= , CM000681.2:g.40848286T= GRCh38
NC_000019.9:g.41354191T= , CM000681.1:g.41354191T= GRCh37
NC_000019.8:g.46046031T= NCBI36
NG_008377.1:g.7162A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301141.10:c.587A= MANE Select ENSP00000301141.4:p.Lys196=
ENST00000301141.9:c.587A= ENSP00000301141.4:p.Lys196=
ENST00000596719.5:n.438A=
ENST00000600495.1:c.*399A= ENSP00000472905.1:n.*399A=
ENST00000601627.1:c.120-43705T=
ENST00000610301.1:c.587A= ENSP00000477899.1:p.Lys196=
NM_000762.5:c.587A= NP_000753.3:p.Lys196=
NM_000762.6:c.587A= MANE Select NP_000753.3:p.Lys196=