Canonical Allele Identifier: CA405965377

Gene: CYP2A6

Linked Data

• MyVariant Identifiers: chr19:g.41354203T>A (hg19) ; chr19:g.40848298T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40848298T>A , CM000681.2:g.40848298T>A	GRCh38
NC_000019.9:g.41354203T>A , CM000681.1:g.41354203T>A	GRCh37
NC_000019.8:g.46046043T>A	NCBI36
NG_008377.1:g.7150A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301141.10:c.575A>T MANE Select	ENSP00000301141.4:p.Asp192Val
ENST00000301141.9:c.575A>T	ENSP00000301141.4:p.Asp192Val
ENST00000596719.5:n.426A>T
ENST00000600495.1:c.*387A>T	ENSP00000472905.1:n.*387A>T
ENST00000601627.1:c.120-43693T>A
ENST00000610301.1:c.575A>T	ENSP00000477899.1:p.Asp192Val
NM_000762.5:c.575A>T	NP_000753.3:p.Asp192Val
NM_000762.6:c.575A>T MANE Select	NP_000753.3:p.Asp192Val