Canonical Allele Identifier: CA2336176382
Gene: CYP2A6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40843766C= , CM000681.2:g.40843766C= GRCh38
NC_000019.9:g.41349671C= , CM000681.1:g.41349671C= GRCh37
NC_000019.8:g.46041511C= NCBI36
NG_008377.1:g.11682G=

Transcript Alleles

HGVS Amino-acid change
ENST00000301141.10:c.*30G= MANE Select ENSP00000301141.4:n.*30G=
ENST00000301141.9:c.*30G= ENSP00000301141.4:n.*30G=
ENST00000599960.1:n.434G=
ENST00000601627.1:c.119+42351C=
NM_000762.5:c.*30G= NP_000753.3:n.*30G=
NM_000762.6:c.*30G= MANE Select NP_000753.3:n.*30G=