Canonical Allele Identifier: CA2336178793
Gene: CYP2A6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40848276C= , CM000681.2:g.40848276C= GRCh38
NC_000019.9:g.41354181C= , CM000681.1:g.41354181C= GRCh37
NC_000019.8:g.46046021C= NCBI36
NG_008377.1:g.7172G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301141.10:c.597G= MANE Select ENSP00000301141.4:p.Leu199=
ENST00000301141.9:c.597G= ENSP00000301141.4:p.Leu199=
ENST00000596719.5:n.448G=
ENST00000600495.1:c.*409G= ENSP00000472905.1:n.*409G=
ENST00000601627.1:c.120-43715C=
ENST00000610301.1:c.597G= ENSP00000477899.1:p.Leu199=
NM_000762.5:c.597G= NP_000753.3:p.Leu199=
NM_000762.6:c.597G= MANE Select NP_000753.3:p.Leu199=