Canonical Allele Identifier: CA920110353

Gene: CYP2A6

Linked Data

• dbSNP Id: rs1599777197
• gnomAD v3: 19-40844988-G-GT
• gnomAD v4: 19-40844988-G-GT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40844988_40844989insT , CM000681.2:g.40844988_40844989insT	GRCh38
NC_000019.9:g.41350893_41350894insT , CM000681.1:g.41350893_41350894insT	GRCh37
NC_000019.8:g.46042733_46042734insT	NCBI36
NG_008377.1:g.10459_10460insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301141.10:c.1162-217_1162-216insA MANE Select	ENSP00000301141.4:n.1162-217_1162-216insA
ENST00000301141.9:c.1162-217_1162-216insA	ENSP00000301141.4:n.1162-217_1162-216insA
ENST00000596719.5:n.1317_1318insA
ENST00000601627.1:c.119+43573_119+43574insT
ENST00000610301.1:c.1162-217_1162-216insA	ENSP00000477899.1:n.1162-217_1162-216insA
NM_000762.5:c.1162-217_1162-216insA	NP_000753.3:n.1162-217_1162-216insA
NM_000762.6:c.1162-217_1162-216insA MANE Select	NP_000753.3:n.1162-217_1162-216insA