Canonical Allele Identifier: CA2336178659

Gene: CYP2A6

Linked Data

• dbSNP Id: rs1967131222

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40848053_40848064del , CM000681.2:g.40848053_40848064del	GRCh38
NC_000019.9:g.41353958_41353969del , CM000681.1:g.41353958_41353969del	GRCh37
NC_000019.8:g.46045798_46045809del	NCBI36
NG_008377.1:g.7384_7395del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301141.10:c.654+155_654+166del MANE Select	ENSP00000301141.4:n.654+155_654+166del
ENST00000301141.9:c.654+155_654+166del	ENSP00000301141.4:n.654+155_654+166del
ENST00000596719.5:n.505+155_505+166del
ENST00000600495.1:c.*466+155_*466+166del	ENSP00000472905.1:n.*466+155_*466+166del
ENST00000601627.1:c.120-43938_120-43927del
ENST00000610301.1:c.654+155_654+166del	ENSP00000477899.1:n.654+155_654+166del
NM_000762.5:c.654+155_654+166del	NP_000753.3:n.654+155_654+166del
NM_000762.6:c.654+155_654+166del MANE Select	NP_000753.3:n.654+155_654+166del