Canonical Allele Identifier: CA2336178700
Gene: CYP2A6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40848127G= , CM000681.2:g.40848127G= GRCh38
NC_000019.9:g.41354032G= , CM000681.1:g.41354032G= GRCh37
NC_000019.8:g.46045872G= NCBI36
NG_008377.1:g.7321C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301141.10:c.654+92C= MANE Select ENSP00000301141.4:n.654+92C=
ENST00000301141.9:c.654+92C= ENSP00000301141.4:n.654+92C=
ENST00000596719.5:n.505+92C=
ENST00000600495.1:c.*466+92C= ENSP00000472905.1:n.*466+92C=
ENST00000601627.1:c.120-43864G=
ENST00000610301.1:c.654+92C= ENSP00000477899.1:n.654+92C=
NM_000762.5:c.654+92C= NP_000753.3:n.654+92C=
NM_000762.6:c.654+92C= MANE Select NP_000753.3:n.654+92C=