Canonical Allele Identifier: CA2814417564
Gene: CYP2A6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40848445A>G , CM000681.2:g.40848445A>G GRCh38
NC_000019.9:g.41354350A>G , CM000681.1:g.41354350A>G GRCh37
NC_000019.8:g.46046190A>G NCBI36
NG_008377.1:g.7003T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000301141.10:c.494-66T>C MANE Select ENSP00000301141.4:n.494-66T>C
ENST00000301141.9:c.494-66T>C ENSP00000301141.4:n.494-66T>C
ENST00000596719.5:n.345-66T>C
ENST00000600495.1:c.*306-66T>C ENSP00000472905.1:n.*306-66T>C
ENST00000601627.1:c.120-43546A>G
ENST00000610301.1:c.494-66T>C ENSP00000477899.1:n.494-66T>C
NM_000762.5:c.494-66T>C NP_000753.3:n.494-66T>C
NM_000762.6:c.494-66T>C MANE Select NP_000753.3:n.494-66T>C