Canonical Allele Identifier: CA2814417772
Gene: CYP2A6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40843770C>T , CM000681.2:g.40843770C>T GRCh38
NC_000019.9:g.41349675C>T , CM000681.1:g.41349675C>T GRCh37
NC_000019.8:g.46041515C>T NCBI36
NG_008377.1:g.11678G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000301141.10:c.*26G>A MANE Select ENSP00000301141.4:n.*26G>A
ENST00000301141.9:c.*26G>A ENSP00000301141.4:n.*26G>A
ENST00000599960.1:n.430G>A
ENST00000601627.1:c.119+42355C>T
NM_000762.5:c.*26G>A NP_000753.3:n.*26G>A
NM_000762.6:c.*26G>A MANE Select NP_000753.3:n.*26G>A