Canonical Allele Identifier: CA2585205047
Gene: CYP2A6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40848465G>C , CM000681.2:g.40848465G>C GRCh38
NC_000019.9:g.41354370G>C , CM000681.1:g.41354370G>C GRCh37
NC_000019.8:g.46046210G>C NCBI36
NG_008377.1:g.6983C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000301141.10:c.494-86C>G MANE Select ENSP00000301141.4:n.494-86C>G
ENST00000301141.9:c.494-86C>G ENSP00000301141.4:n.494-86C>G
ENST00000596719.5:n.345-86C>G
ENST00000600495.1:c.*306-86C>G ENSP00000472905.1:n.*306-86C>G
ENST00000601627.1:c.120-43526G>C
ENST00000610301.1:c.494-86C>G ENSP00000477899.1:n.494-86C>G
NM_000762.5:c.494-86C>G NP_000753.3:n.494-86C>G
NM_000762.6:c.494-86C>G MANE Select NP_000753.3:n.494-86C>G