Canonical Allele Identifier: CA2336178653

Gene: CYP2A6

Linked Data

• dbSNP Id: rs1967130028

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40848044_40848051del , CM000681.2:g.40848044_40848051del	GRCh38
NC_000019.9:g.41353949_41353956del , CM000681.1:g.41353949_41353956del	GRCh37
NC_000019.8:g.46045789_46045796del	NCBI36
NG_008377.1:g.7397_7404del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301141.10:c.654+168_654+175del MANE Select	ENSP00000301141.4:n.654+168_654+175del
ENST00000301141.9:c.654+168_654+175del	ENSP00000301141.4:n.654+168_654+175del
ENST00000596719.5:n.505+168_505+175del
ENST00000600495.1:c.*466+168_*466+175del	ENSP00000472905.1:n.*466+168_*466+175del
ENST00000601627.1:c.120-43947_120-43940del
ENST00000610301.1:c.654+168_654+175del	ENSP00000477899.1:n.654+168_654+175del
NM_000762.5:c.654+168_654+175del	NP_000753.3:n.654+168_654+175del
NM_000762.6:c.654+168_654+175del MANE Select	NP_000753.3:n.654+168_654+175del