Canonical Allele Identifier: CA2336178689

Gene: CYP2A6

Linked Data

• dbSNP Id: rs1967132088

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40848113_40848114del , CM000681.2:g.40848113_40848114del	GRCh38
NC_000019.9:g.41354018_41354019del , CM000681.1:g.41354018_41354019del	GRCh37
NC_000019.8:g.46045858_46045859del	NCBI36
NG_008377.1:g.7336_7337del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301141.10:c.654+107_654+108del MANE Select	ENSP00000301141.4:n.654+107_654+108del
ENST00000301141.9:c.654+107_654+108del	ENSP00000301141.4:n.654+107_654+108del
ENST00000596719.5:n.505+107_505+108del
ENST00000600495.1:c.*466+107_*466+108del	ENSP00000472905.1:n.*466+107_*466+108del
ENST00000601627.1:c.120-43878_120-43877del
ENST00000610301.1:c.654+107_654+108del	ENSP00000477899.1:n.654+107_654+108del
NM_000762.5:c.654+107_654+108del	NP_000753.3:n.654+107_654+108del
NM_000762.6:c.654+107_654+108del MANE Select	NP_000753.3:n.654+107_654+108del