Canonical Allele Identifier: CA2336177067
Gene: CYP2A6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40845019T= , CM000681.2:g.40845019T= GRCh38
NC_000019.9:g.41350924T= , CM000681.1:g.41350924T= GRCh37
NC_000019.8:g.46042764T= NCBI36
NG_008377.1:g.10429A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301141.10:c.1162-247A= MANE Select ENSP00000301141.4:n.1162-247A=
ENST00000301141.9:c.1162-247A= ENSP00000301141.4:n.1162-247A=
ENST00000596719.5:n.1287A=
ENST00000601627.1:c.119+43604T=
ENST00000610301.1:c.1162-247A= ENSP00000477899.1:n.1162-247A=
NM_000762.5:c.1162-247A= NP_000753.3:n.1162-247A=
NM_000762.6:c.1162-247A= MANE Select NP_000753.3:n.1162-247A=