Canonical Allele Identifier: CA2336176331
Gene: CYP2A6 HGNC NCBI

Linked Data

dbSNP Id: rs2083441309

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40843715_40843716insAC , CM000681.2:g.40843715_40843716insAC GRCh38
NC_000019.9:g.41349620_41349621insAC , CM000681.1:g.41349620_41349621insAC GRCh37
NC_000019.8:g.46041460_46041461insAC NCBI36
NG_008377.1:g.11732_11733insGT

Transcript Alleles

HGVS Amino-acid change
ENST00000301141.10:c.*80_*81insGT MANE Select ENSP00000301141.4:n.*80_*81insGT
ENST00000301141.9:c.*80_*81insGT ENSP00000301141.4:n.*80_*81insGT
ENST00000599960.1:n.484_485insGT
ENST00000601627.1:c.119+42300_119+42301insAC
NM_000762.5:c.*80_*81insGT NP_000753.3:n.*80_*81insGT
NM_000762.6:c.*80_*81insGT MANE Select NP_000753.3:n.*80_*81insGT