Canonical Allele Identifier: CA2336177171
Gene: CYP2A6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40845190G= , CM000681.2:g.40845190G= GRCh38
NC_000019.9:g.41351095G= , CM000681.1:g.41351095G= GRCh37
NC_000019.8:g.46042935G= NCBI36
NG_008377.1:g.10258C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301141.10:c.1161+104C= MANE Select ENSP00000301141.4:n.1161+104C=
ENST00000301141.9:c.1161+104C= ENSP00000301141.4:n.1161+104C=
ENST00000596719.5:n.1116C=
ENST00000601627.1:c.119+43775G=
ENST00000610301.1:c.1161+104C= ENSP00000477899.1:n.1161+104C=
NM_000762.5:c.1161+104C= NP_000753.3:n.1161+104C=
NM_000762.6:c.1161+104C= MANE Select NP_000753.3:n.1161+104C=