Canonical Allele Identifier: CA2336178887
Gene: CYP2A6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40848441C= , CM000681.2:g.40848441C= GRCh38
NC_000019.9:g.41354346C= , CM000681.1:g.41354346C= GRCh37
NC_000019.8:g.46046186C= NCBI36
NG_008377.1:g.7007G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301141.10:c.494-62G= MANE Select ENSP00000301141.4:n.494-62G=
ENST00000301141.9:c.494-62G= ENSP00000301141.4:n.494-62G=
ENST00000596719.5:n.345-62G=
ENST00000600495.1:c.*306-62G= ENSP00000472905.1:n.*306-62G=
ENST00000601627.1:c.120-43550C=
ENST00000610301.1:c.494-62G= ENSP00000477899.1:n.494-62G=
NM_000762.5:c.494-62G= NP_000753.3:n.494-62G=
NM_000762.6:c.494-62G= MANE Select NP_000753.3:n.494-62G=