Canonical Allele Identifier: CA2336177089
Gene: CYP2A6 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40845064G= , CM000681.2:g.40845064G= GRCh38
NC_000019.9:g.41350969G= , CM000681.1:g.41350969G= GRCh37
NC_000019.8:g.46042809G= NCBI36
NG_008377.1:g.10384C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301141.10:c.1161+230C= MANE Select ENSP00000301141.4:n.1161+230C=
ENST00000301141.9:c.1161+230C= ENSP00000301141.4:n.1161+230C=
ENST00000596719.5:n.1242C=
ENST00000601627.1:c.119+43649G=
ENST00000610301.1:c.1161+230C= ENSP00000477899.1:n.1161+230C=
NM_000762.5:c.1161+230C= NP_000753.3:n.1161+230C=
NM_000762.6:c.1161+230C= MANE Select NP_000753.3:n.1161+230C=
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