Canonical Allele Identifier: CA9453042
Gene: CYP2A6 HGNC NCBI

Linked Data

dbSNP Id: rs758215581
ExAC: 19:41354278 T / C
gnomAD v2: 19-41354278-T-C
gnomAD v4: 19-40848373-T-C
MyVariant Identifiers: chr19:g.41354278T>C (hg19) chr19:g.40848373T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40848373T>C , CM000681.2:g.40848373T>C GRCh38
NC_000019.9:g.41354278T>C , CM000681.1:g.41354278T>C GRCh37
NC_000019.8:g.46046118T>C NCBI36
NG_008377.1:g.7075A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000301141.10:c.500A>G MANE Select ENSP00000301141.4:p.Asn167Ser
ENST00000301141.9:c.500A>G ENSP00000301141.4:p.Asn167Ser
ENST00000596719.5:n.351A>G
ENST00000600495.1:c.*312A>G ENSP00000472905.1:n.*312A>G
ENST00000601627.1:c.120-43618T>C
ENST00000610301.1:c.500A>G ENSP00000477899.1:p.Asn167Ser
NM_000762.5:c.500A>G NP_000753.3:p.Asn167Ser
NM_000762.6:c.500A>G MANE Select NP_000753.3:p.Asn167Ser
Search 100 bp 5'
Search 100 bp 3'