Canonical Allele Identifier: CA308456585

Gene: CYP2A6

Linked Data

• dbSNP Id: rs879374863

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40848400_40848401delinsA , CM000681.2:g.40848400_40848401delinsA	GRCh38
NC_000019.9:g.41354305_41354306delinsA , CM000681.1:g.41354305_41354306delinsA	GRCh37
NC_000019.8:g.46046145_46046146delinsA	NCBI36
NG_008377.1:g.7047_7048delinsT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301141.10:c.494-22_494-21delinsT MANE Select	ENSP00000301141.4:n.494-22_494-21delinsT
ENST00000301141.9:c.494-22_494-21delinsT	ENSP00000301141.4:n.494-22_494-21delinsT
ENST00000596719.5:n.345-22_345-21delinsT
ENST00000600495.1:c.*306-22_*306-21delinsT	ENSP00000472905.1:n.*306-22_*306-21delinsT
ENST00000601627.1:c.120-43591_120-43590delinsA
ENST00000610301.1:c.494-22_494-21delinsT	ENSP00000477899.1:n.494-22_494-21delinsT
NM_000762.5:c.494-22_494-21delinsT	NP_000753.3:n.494-22_494-21delinsT
NM_000762.6:c.494-22_494-21delinsT MANE Select	NP_000753.3:n.494-22_494-21delinsT