Canonical Allele Identifier: CA405965624

Gene: CYP2A6

Linked Data

• dbSNP Id: rs1967143589
• MyVariant Identifiers: chr19:g.41354545A>T (hg19) ; chr19:g.40848640A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40848640A>T , CM000681.2:g.40848640A>T	GRCh38
NC_000019.9:g.41354545A>T , CM000681.1:g.41354545A>T	GRCh37
NC_000019.8:g.46046385A>T	NCBI36
NG_008377.1:g.6808T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000301141.10:c.467T>A MANE Select	ENSP00000301141.4:p.Leu156His
ENST00000301141.9:c.467T>A	ENSP00000301141.4:p.Leu156His
ENST00000596719.5:n.318T>A
ENST00000600495.1:c.*279T>A	ENSP00000472905.1:n.*279T>A
ENST00000601627.1:c.120-43351A>T
ENST00000610301.1:c.467T>A	ENSP00000477899.1:p.Leu156His
NM_000762.5:c.467T>A	NP_000753.3:p.Leu156His
NM_000762.6:c.467T>A MANE Select	NP_000753.3:p.Leu156His