Canonical Allele Identifier: CA405965562
Gene: CYP2A6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40848374T>C , CM000681.2:g.40848374T>C GRCh38
NC_000019.9:g.41354279T>C , CM000681.1:g.41354279T>C GRCh37
NC_000019.8:g.46046119T>C NCBI36
NG_008377.1:g.7074A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000301141.10:c.499A>G MANE Select ENSP00000301141.4:p.Asn167Asp
ENST00000301141.9:c.499A>G ENSP00000301141.4:p.Asn167Asp
ENST00000596719.5:n.350A>G
ENST00000600495.1:c.*311A>G ENSP00000472905.1:n.*311A>G
ENST00000601627.1:c.120-43617T>C
ENST00000610301.1:c.499A>G ENSP00000477899.1:p.Asn167Asp
NM_000762.5:c.499A>G NP_000753.3:p.Asn167Asp
NM_000762.6:c.499A>G MANE Select NP_000753.3:p.Asn167Asp