Canonical Allele Identifier: CA2336177132
Gene: CYP2A6 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40845152G= , CM000681.2:g.40845152G= GRCh38
NC_000019.9:g.41351057G= , CM000681.1:g.41351057G= GRCh37
NC_000019.8:g.46042897G= NCBI36
NG_008377.1:g.10296C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301141.10:c.1161+142C= MANE Select ENSP00000301141.4:n.1161+142C=
ENST00000301141.9:c.1161+142C= ENSP00000301141.4:n.1161+142C=
ENST00000596719.5:n.1154C=
ENST00000601627.1:c.119+43737G=
ENST00000610301.1:c.1161+142C= ENSP00000477899.1:n.1161+142C=
NM_000762.5:c.1161+142C= NP_000753.3:n.1161+142C=
NM_000762.6:c.1161+142C= MANE Select NP_000753.3:n.1161+142C=
Search 100 bp 5'
Search 100 bp 3'