Canonical Allele Identifier: CA2336177106

Gene: CYP2A6

Linked Data

• dbSNP Id: rs2083448900

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40845100_40845101del , CM000681.2:g.40845100_40845101del	GRCh38
NC_000019.9:g.41351005_41351006del , CM000681.1:g.41351005_41351006del	GRCh37
NC_000019.8:g.46042845_46042846del	NCBI36
NG_008377.1:g.10348_10349del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301141.10:c.1161+194_1161+195del MANE Select	ENSP00000301141.4:n.1161+194_1161+195del
ENST00000301141.9:c.1161+194_1161+195del	ENSP00000301141.4:n.1161+194_1161+195del
ENST00000596719.5:n.1206_1207del
ENST00000601627.1:c.119+43685_119+43686del
ENST00000610301.1:c.1161+194_1161+195del	ENSP00000477899.1:n.1161+194_1161+195del
NM_000762.5:c.1161+194_1161+195del	NP_000753.3:n.1161+194_1161+195del
NM_000762.6:c.1161+194_1161+195del MANE Select	NP_000753.3:n.1161+194_1161+195del