Canonical Allele Identifier: CA405965371
Gene: CYP2A6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40848295T>G , CM000681.2:g.40848295T>G GRCh38
NC_000019.9:g.41354200T>G , CM000681.1:g.41354200T>G GRCh37
NC_000019.8:g.46046040T>G NCBI36
NG_008377.1:g.7153A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000301141.10:c.578A>C MANE Select ENSP00000301141.4:p.Tyr193Ser
ENST00000301141.9:c.578A>C ENSP00000301141.4:p.Tyr193Ser
ENST00000596719.5:n.429A>C
ENST00000600495.1:c.*390A>C ENSP00000472905.1:n.*390A>C
ENST00000601627.1:c.120-43696T>G
ENST00000610301.1:c.578A>C ENSP00000477899.1:p.Tyr193Ser
NM_000762.5:c.578A>C NP_000753.3:p.Tyr193Ser
NM_000762.6:c.578A>C MANE Select NP_000753.3:p.Tyr193Ser