Canonical Allele Identifier: CA2336178640
Gene: CYP2A6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40848027G= , CM000681.2:g.40848027G= GRCh38
NC_000019.9:g.41353932G= , CM000681.1:g.41353932G= GRCh37
NC_000019.8:g.46045772G= NCBI36
NG_008377.1:g.7421C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301141.10:c.654+192C= MANE Select ENSP00000301141.4:n.654+192C=
ENST00000301141.9:c.654+192C= ENSP00000301141.4:n.654+192C=
ENST00000596719.5:n.505+192C=
ENST00000600495.1:c.*466+192C= ENSP00000472905.1:n.*466+192C=
ENST00000601627.1:c.120-43964G=
ENST00000610301.1:c.654+192C= ENSP00000477899.1:n.654+192C=
NM_000762.5:c.654+192C= NP_000753.3:n.654+192C=
NM_000762.6:c.654+192C= MANE Select NP_000753.3:n.654+192C=