Canonical Allele Identifier: CA2336178869
Gene: CYP2A6 HGNC NCBI

Linked Data

dbSNP Id: rs1568515561

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40848402G>A , CM000681.2:g.40848402G>A GRCh38
NC_000019.9:g.41354307G>A , CM000681.1:g.41354307G>A GRCh37
NC_000019.8:g.46046147G>A NCBI36
NG_008377.1:g.7046C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000301141.10:c.494-23C>T MANE Select ENSP00000301141.4:n.494-23C>T
ENST00000301141.9:c.494-23C>T ENSP00000301141.4:n.494-23C>T
ENST00000596719.5:n.345-23C>T
ENST00000600495.1:c.*306-23C>T ENSP00000472905.1:n.*306-23C>T
ENST00000601627.1:c.120-43589G>A
ENST00000610301.1:c.494-23C>T ENSP00000477899.1:n.494-23C>T
NM_000762.5:c.494-23C>T NP_000753.3:n.494-23C>T
NM_000762.6:c.494-23C>T MANE Select NP_000753.3:n.494-23C>T