Canonical Allele Identifier: CA2336178949
Gene: CYP2A6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40848562C= , CM000681.2:g.40848562C= GRCh38
NC_000019.9:g.41354467C= , CM000681.1:g.41354467C= GRCh37
NC_000019.8:g.46046307C= NCBI36
NG_008377.1:g.6886G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301141.10:c.493+52G= MANE Select ENSP00000301141.4:n.493+52G=
ENST00000301141.9:c.493+52G= ENSP00000301141.4:n.493+52G=
ENST00000596719.5:n.344+52G=
ENST00000600495.1:c.*305+52G= ENSP00000472905.1:n.*305+52G=
ENST00000601627.1:c.120-43429C=
ENST00000610301.1:c.493+52G= ENSP00000477899.1:n.493+52G=
NM_000762.5:c.493+52G= NP_000753.3:n.493+52G=
NM_000762.6:c.493+52G= MANE Select NP_000753.3:n.493+52G=