Canonical Allele Identifier: CA2336176380
Gene: CYP2A6 HGNC NCBI

Linked Data

dbSNP Id: rs768823423

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40843765C>T , CM000681.2:g.40843765C>T GRCh38
NC_000019.9:g.41349670C>T , CM000681.1:g.41349670C>T GRCh37
NC_000019.8:g.46041510C>T NCBI36
NG_008377.1:g.11683G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000301141.10:c.*31G>A MANE Select ENSP00000301141.4:n.*31G>A
ENST00000301141.9:c.*31G>A ENSP00000301141.4:n.*31G>A
ENST00000599960.1:n.435G>A
ENST00000601627.1:c.119+42350C>T
NM_000762.5:c.*31G>A NP_000753.3:n.*31G>A
NM_000762.6:c.*31G>A MANE Select NP_000753.3:n.*31G>A