Canonical Allele Identifier: CA2336176301
Gene: CYP2A6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40843676A= , CM000681.2:g.40843676A= GRCh38
NC_000019.9:g.41349581A= , CM000681.1:g.41349581A= GRCh37
NC_000019.8:g.46041421A= NCBI36
NG_008377.1:g.11772T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301141.10:c.*120T= MANE Select ENSP00000301141.4:n.*120T=
ENST00000301141.9:c.*120T= ENSP00000301141.4:n.*120T=
ENST00000599960.1:n.524T=
ENST00000601627.1:c.119+42261A=
NM_000762.5:c.*120T= NP_000753.3:n.*120T=
NM_000762.6:c.*120T= MANE Select NP_000753.3:n.*120T=