Canonical Allele Identifier: CA2336178851
Gene: CYP2A6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40848387T= , CM000681.2:g.40848387T= GRCh38
NC_000019.9:g.41354292T= , CM000681.1:g.41354292T= GRCh37
NC_000019.8:g.46046132T= NCBI36
NG_008377.1:g.7061A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301141.10:c.494-8A= MANE Select ENSP00000301141.4:n.494-8A=
ENST00000301141.9:c.494-8A= ENSP00000301141.4:n.494-8A=
ENST00000596719.5:n.345-8A=
ENST00000600495.1:c.*306-8A= ENSP00000472905.1:n.*306-8A=
ENST00000601627.1:c.120-43604T=
ENST00000610301.1:c.494-8A= ENSP00000477899.1:n.494-8A=
NM_000762.5:c.494-8A= NP_000753.3:n.494-8A=
NM_000762.6:c.494-8A= MANE Select NP_000753.3:n.494-8A=