Canonical Allele Identifier: CA2336177158

Gene: CYP2A6

Linked Data

• dbSNP Id: rs2083449473

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40845175T>C , CM000681.2:g.40845175T>C	GRCh38
NC_000019.9:g.41351080T>C , CM000681.1:g.41351080T>C	GRCh37
NC_000019.8:g.46042920T>C	NCBI36
NG_008377.1:g.10273A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301141.10:c.1161+119A>G MANE Select	ENSP00000301141.4:n.1161+119A>G
ENST00000301141.9:c.1161+119A>G	ENSP00000301141.4:n.1161+119A>G
ENST00000596719.5:n.1131A>G
ENST00000601627.1:c.119+43760T>C
ENST00000610301.1:c.1161+119A>G	ENSP00000477899.1:n.1161+119A>G
NM_000762.5:c.1161+119A>G	NP_000753.3:n.1161+119A>G
NM_000762.6:c.1161+119A>G MANE Select	NP_000753.3:n.1161+119A>G