Canonical Allele Identifier: CA9452765

Gene: CYP2A6

Linked Data

• dbSNP Id: rs28399455
• ExAC: 19:41351190 G / A
• gnomAD v2: 19-41351190-G-A
• gnomAD v3: 19-40845285-G-A
• gnomAD v4: 19-40845285-G-A
• MyVariant Identifiers: chr19:g.41351190G>A (hg19) ; chr19:g.40845285G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40845285G>A , CM000681.2:g.40845285G>A	GRCh38
NC_000019.9:g.41351190G>A , CM000681.1:g.41351190G>A	GRCh37
NC_000019.8:g.46043030G>A	NCBI36
NG_008377.1:g.10163C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301141.10:c.1161+9C>T MANE Select	ENSP00000301141.4:n.1161+9C>T
ENST00000301141.9:c.1161+9C>T	ENSP00000301141.4:n.1161+9C>T
ENST00000596719.5:n.1021C>T
ENST00000601627.1:c.119+43870G>A
ENST00000610301.1:c.1161+9C>T	ENSP00000477899.1:n.1161+9C>T
NM_000762.5:c.1161+9C>T	NP_000753.3:n.1161+9C>T
NM_000762.6:c.1161+9C>T MANE Select	NP_000753.3:n.1161+9C>T