Canonical Allele Identifier: CA507688189

Gene: CYP2A6

Linked Data

• dbSNP Id: rs762417955
• MyVariant Identifiers: chr19:g.41354541G>A (hg19) ; chr19:g.40848636G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40848636G>A , CM000681.2:g.40848636G>A	GRCh38
NC_000019.9:g.41354541G>A , CM000681.1:g.41354541G>A	GRCh37
NC_000019.8:g.46046381G>A	NCBI36
NG_008377.1:g.6812C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000301141.10:c.471C>T MANE Select	ENSP00000301141.4:p.Ile157=
ENST00000301141.9:c.471C>T	ENSP00000301141.4:p.Ile157=
ENST00000596719.5:n.322C>T
ENST00000600495.1:c.*283C>T	ENSP00000472905.1:n.*283C>T
ENST00000601627.1:c.120-43355G>A
ENST00000610301.1:c.471C>T	ENSP00000477899.1:p.Ile157=
NM_000762.5:c.471C>T	NP_000753.3:p.Ile157=
NM_000762.6:c.471C>T MANE Select	NP_000753.3:p.Ile157=