Canonical Allele Identifier: CA405961974

Gene: CYP2A6

Linked Data

• MyVariant Identifiers: chr19:g.41351245C>A (hg19) ; chr19:g.40845340C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40845340C>A , CM000681.2:g.40845340C>A	GRCh38
NC_000019.9:g.41351245C>A , CM000681.1:g.41351245C>A	GRCh37
NC_000019.8:g.46043085C>A	NCBI36
NG_008377.1:g.10108G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301141.10:c.1115G>T MANE Select	ENSP00000301141.4:p.Arg372Leu
ENST00000301141.9:c.1115G>T	ENSP00000301141.4:p.Arg372Leu
ENST00000596719.5:n.966G>T
ENST00000601627.1:c.119+43925C>A
ENST00000610301.1:c.1115G>T	ENSP00000477899.1:p.Arg372Leu
NM_000762.5:c.1115G>T	NP_000753.3:p.Arg372Leu
NM_000762.6:c.1115G>T MANE Select	NP_000753.3:p.Arg372Leu