Canonical Allele Identifier: CA2336177070
Gene: CYP2A6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40845026A= , CM000681.2:g.40845026A= GRCh38
NC_000019.9:g.41350931A= , CM000681.1:g.41350931A= GRCh37
NC_000019.8:g.46042771A= NCBI36
NG_008377.1:g.10422T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301141.10:c.1162-254T= MANE Select ENSP00000301141.4:n.1162-254T=
ENST00000301141.9:c.1162-254T= ENSP00000301141.4:n.1162-254T=
ENST00000596719.5:n.1280T=
ENST00000601627.1:c.119+43611A=
ENST00000610301.1:c.1162-254T= ENSP00000477899.1:n.1162-254T=
NM_000762.5:c.1162-254T= NP_000753.3:n.1162-254T=
NM_000762.6:c.1162-254T= MANE Select NP_000753.3:n.1162-254T=