Canonical Allele Identifier: CA2336177169
Gene: CYP2A6 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40845189A= , CM000681.2:g.40845189A= GRCh38
NC_000019.9:g.41351094A= , CM000681.1:g.41351094A= GRCh37
NC_000019.8:g.46042934A= NCBI36
NG_008377.1:g.10259T=

Transcript Alleles

HGVS Amino-acid change
ENST00000301141.10:c.1161+105T= MANE Select ENSP00000301141.4:n.1161+105T=
ENST00000301141.9:c.1161+105T= ENSP00000301141.4:n.1161+105T=
ENST00000596719.5:n.1117T=
ENST00000601627.1:c.119+43774A=
ENST00000610301.1:c.1161+105T= ENSP00000477899.1:n.1161+105T=
NM_000762.5:c.1161+105T= NP_000753.3:n.1161+105T=
NM_000762.6:c.1161+105T= MANE Select NP_000753.3:n.1161+105T=
Search 100 bp 5'
Search 100 bp 3'