Canonical Allele Identifier: CA405965427
Gene: CYP2A6 HGNC NCBI

Linked Data

dbSNP Id: rs1967136172

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40848316A>G , CM000681.2:g.40848316A>G GRCh38
NC_000019.9:g.41354221A>G , CM000681.1:g.41354221A>G GRCh37
NC_000019.8:g.46046061A>G NCBI36
NG_008377.1:g.7132T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000301141.10:c.557T>C MANE Select ENSP00000301141.4:p.Val186Ala
ENST00000301141.9:c.557T>C ENSP00000301141.4:p.Val186Ala
ENST00000596719.5:n.408T>C
ENST00000600495.1:c.*369T>C ENSP00000472905.1:n.*369T>C
ENST00000601627.1:c.120-43675A>G
ENST00000610301.1:c.557T>C ENSP00000477899.1:p.Val186Ala
NM_000762.5:c.557T>C NP_000753.3:p.Val186Ala
NM_000762.6:c.557T>C MANE Select NP_000753.3:p.Val186Ala