Canonical Allele Identifier: CA405965417
Gene: CYP2A6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40848313A>C , CM000681.2:g.40848313A>C GRCh38
NC_000019.9:g.41354218A>C , CM000681.1:g.41354218A>C GRCh37
NC_000019.8:g.46046058A>C NCBI36
NG_008377.1:g.7135T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000301141.10:c.560T>G MANE Select ENSP00000301141.4:p.Phe187Cys
ENST00000301141.9:c.560T>G ENSP00000301141.4:p.Phe187Cys
ENST00000596719.5:n.411T>G
ENST00000600495.1:c.*372T>G ENSP00000472905.1:n.*372T>G
ENST00000601627.1:c.120-43678A>C
ENST00000610301.1:c.560T>G ENSP00000477899.1:p.Phe187Cys
NM_000762.5:c.560T>G NP_000753.3:p.Phe187Cys
NM_000762.6:c.560T>G MANE Select NP_000753.3:p.Phe187Cys