Canonical Allele Identifier: CA2585204990
Gene: CYP2A6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40848154T>C , CM000681.2:g.40848154T>C GRCh38
NC_000019.9:g.41354059T>C , CM000681.1:g.41354059T>C GRCh37
NC_000019.8:g.46045899T>C NCBI36
NG_008377.1:g.7294A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000301141.10:c.654+65A>G MANE Select ENSP00000301141.4:n.654+65A>G
ENST00000301141.9:c.654+65A>G ENSP00000301141.4:n.654+65A>G
ENST00000596719.5:n.505+65A>G
ENST00000600495.1:c.*466+65A>G ENSP00000472905.1:n.*466+65A>G
ENST00000601627.1:c.120-43837T>C
ENST00000610301.1:c.654+65A>G ENSP00000477899.1:n.654+65A>G
NM_000762.5:c.654+65A>G NP_000753.3:n.654+65A>G
NM_000762.6:c.654+65A>G MANE Select NP_000753.3:n.654+65A>G