Canonical Allele Identifier: CA405965339
Gene: CYP2A6 HGNC NCBI

Linked Data

dbSNP Id: rs1967135718
MyVariant Identifiers: chr19:g.41354191T>C (hg19) chr19:g.40848286T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40848286T>C , CM000681.2:g.40848286T>C GRCh38
NC_000019.9:g.41354191T>C , CM000681.1:g.41354191T>C GRCh37
NC_000019.8:g.46046031T>C NCBI36
NG_008377.1:g.7162A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000301141.10:c.587A>G MANE Select ENSP00000301141.4:p.Lys196Arg
ENST00000301141.9:c.587A>G ENSP00000301141.4:p.Lys196Arg
ENST00000596719.5:n.438A>G
ENST00000600495.1:c.*399A>G ENSP00000472905.1:n.*399A>G
ENST00000601627.1:c.120-43705T>C
ENST00000610301.1:c.587A>G ENSP00000477899.1:p.Lys196Arg
NM_000762.5:c.587A>G NP_000753.3:p.Lys196Arg
NM_000762.6:c.587A>G MANE Select NP_000753.3:p.Lys196Arg
Search 100 bp 5'
Search 100 bp 3'