Canonical Allele Identifier: CA9453026
Gene: CYP2A6 HGNC NCBI

Linked Data

dbSNP Id: rs199916117
ExAC: 19:41354198 T / C
gnomAD v2: 19-41354198-T-C
gnomAD v3: 19-40848293-T-C
gnomAD v4: 19-40848293-T-C
COSMIC: COSM1129845
MyVariant Identifiers: chr19:g.41354198T>C (hg19) chr19:g.40848293T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40848293T>C , CM000681.2:g.40848293T>C GRCh38
NC_000019.9:g.41354198T>C , CM000681.1:g.41354198T>C GRCh37
NC_000019.8:g.46046038T>C NCBI36
NG_008377.1:g.7155A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000301141.10:c.580A>G MANE Select ENSP00000301141.4:p.Lys194Glu
ENST00000301141.9:c.580A>G ENSP00000301141.4:p.Lys194Glu
ENST00000596719.5:n.431A>G
ENST00000600495.1:c.*392A>G ENSP00000472905.1:n.*392A>G
ENST00000601627.1:c.120-43698T>C
ENST00000610301.1:c.580A>G ENSP00000477899.1:p.Lys194Glu
NM_000762.5:c.580A>G NP_000753.3:p.Lys194Glu
NM_000762.6:c.580A>G MANE Select NP_000753.3:p.Lys194Glu
Search 100 bp 5'
Search 100 bp 3'