Canonical Allele Identifier: CA507688333

Gene: CYP2A6

Linked Data

• MyVariant Identifiers: chr19:g.41354280G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40848375G>T , CM000681.2:g.40848375G>T	GRCh38
NC_000019.9:g.41354280G>T , CM000681.1:g.41354280G>T	GRCh37
NC_000019.8:g.46046120G>T	NCBI36
NG_008377.1:g.7073C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301141.10:c.498C>A MANE Select	ENSP00000301141.4:p.Ala166=
ENST00000301141.9:c.498C>A	ENSP00000301141.4:p.Ala166=
ENST00000596719.5:n.349C>A
ENST00000600495.1:c.*310C>A	ENSP00000472905.1:n.*310C>A
ENST00000601627.1:c.120-43616G>T
ENST00000610301.1:c.498C>A	ENSP00000477899.1:p.Ala166=
NM_000762.5:c.498C>A	NP_000753.3:p.Ala166=
NM_000762.6:c.498C>A MANE Select	NP_000753.3:p.Ala166=