Canonical Allele Identifier: CA882279841

Gene: CYP2A6

Linked Data

• dbSNP Id: rs1254392942
• gnomAD v3: 19-40848461-CCT-C
• gnomAD v4: 19-40848461-CCT-C
• MyVariant Identifiers: chr19:g.41354367_41354368del (hg19) ; chr19:g.40848462_40848463del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40848462_40848463del , CM000681.2:g.40848462_40848463del	GRCh38
NC_000019.9:g.41354367_41354368del , CM000681.1:g.41354367_41354368del	GRCh37
NC_000019.8:g.46046207_46046208del	NCBI36
NG_008377.1:g.6985_6986del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301141.10:c.494-84_494-83del MANE Select	ENSP00000301141.4:n.494-84_494-83del
ENST00000301141.9:c.494-84_494-83del	ENSP00000301141.4:n.494-84_494-83del
ENST00000596719.5:n.345-84_345-83del
ENST00000600495.1:c.*306-84_*306-83del	ENSP00000472905.1:n.*306-84_*306-83del
ENST00000601627.1:c.120-43529_120-43528del
ENST00000610301.1:c.494-84_494-83del	ENSP00000477899.1:n.494-84_494-83del
NM_000762.5:c.494-84_494-83del	NP_000753.3:n.494-84_494-83del
NM_000762.6:c.494-84_494-83del MANE Select	NP_000753.3:n.494-84_494-83del