Canonical Allele Identifier: CA882279500

Gene: CYP2A6

Linked Data

• dbSNP Id: rs1321105302
• MyVariant Identifiers: chr19:g.41354055_41354056insGTCTC (hg19) ; chr19:g.40848150_40848151insGTCTC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40848151_40848155dup , CM000681.2:g.40848151_40848155dup	GRCh38
NC_000019.9:g.41354056_41354060dup , CM000681.1:g.41354056_41354060dup	GRCh37
NC_000019.8:g.46045896_46045900dup	NCBI36
NG_008377.1:g.7293_7297dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301141.10:c.654+64_654+68dup MANE Select	ENSP00000301141.4:n.654+64_654+68dup
ENST00000301141.9:c.654+64_654+68dup	ENSP00000301141.4:n.654+64_654+68dup
ENST00000596719.5:n.505+64_505+68dup
ENST00000600495.1:c.*466+64_*466+68dup	ENSP00000472905.1:n.*466+64_*466+68dup
ENST00000601627.1:c.120-43840_120-43836dup
ENST00000610301.1:c.654+64_654+68dup	ENSP00000477899.1:n.654+64_654+68dup
NM_000762.5:c.654+64_654+68dup	NP_000753.3:n.654+64_654+68dup
NM_000762.6:c.654+64_654+68dup MANE Select	NP_000753.3:n.654+64_654+68dup