Canonical Allele Identifier: CA405965603
Gene: CYP2A6 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.41354533A>G (hg19) chr19:g.40848628A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40848628A>G , CM000681.2:g.40848628A>G GRCh38
NC_000019.9:g.41354533A>G , CM000681.1:g.41354533A>G GRCh37
NC_000019.8:g.46046373A>G NCBI36
NG_008377.1:g.6820T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000301141.10:c.479T>C MANE Select ENSP00000301141.4:p.Leu160Pro
ENST00000301141.9:c.479T>C ENSP00000301141.4:p.Leu160Pro
ENST00000596719.5:n.330T>C
ENST00000600495.1:c.*291T>C ENSP00000472905.1:n.*291T>C
ENST00000601627.1:c.120-43363A>G
ENST00000610301.1:c.479T>C ENSP00000477899.1:p.Leu160Pro
NM_000762.5:c.479T>C NP_000753.3:p.Leu160Pro
NM_000762.6:c.479T>C MANE Select NP_000753.3:p.Leu160Pro
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