Canonical Allele Identifier: CA995923221
Gene: CYP2A6 HGNC NCBI

Linked Data

dbSNP Id: rs2083440687

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40843608C>G , CM000681.2:g.40843608C>G GRCh38
NC_000019.9:g.41349513C>G , CM000681.1:g.41349513C>G GRCh37
NC_000019.8:g.46041353C>G NCBI36
NG_008377.1:g.11840G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000301141.10:c.*188G>C MANE Select ENSP00000301141.4:n.*188G>C
ENST00000301141.9:c.*188G>C ENSP00000301141.4:n.*188G>C
ENST00000599960.1:n.592G>C
ENST00000601627.1:c.119+42193C>G
NM_000762.5:c.*188G>C NP_000753.3:n.*188G>C
NM_000762.6:c.*188G>C MANE Select NP_000753.3:n.*188G>C