Canonical Allele Identifier: CA2814417739
Gene: CYP2A6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40843661T>G , CM000681.2:g.40843661T>G GRCh38
NC_000019.9:g.41349566T>G , CM000681.1:g.41349566T>G GRCh37
NC_000019.8:g.46041406T>G NCBI36
NG_008377.1:g.11787A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000301141.10:c.*135A>C MANE Select ENSP00000301141.4:n.*135A>C
ENST00000301141.9:c.*135A>C ENSP00000301141.4:n.*135A>C
ENST00000599960.1:n.539A>C
ENST00000601627.1:c.119+42246T>G
NM_000762.5:c.*135A>C NP_000753.3:n.*135A>C
NM_000762.6:c.*135A>C MANE Select NP_000753.3:n.*135A>C