Canonical Allele Identifier: CA9453096
Gene: CYP2A6 HGNC NCBI

Linked Data

dbSNP Id: rs772772650
ExAC: 19:41354540 C / T
gnomAD v2: 19-41354540-C-T
gnomAD v3: 19-40848635-C-T
gnomAD v4: 19-40848635-C-T
MyVariant Identifiers: chr19:g.41354540C>T (hg19) chr19:g.40848635C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40848635C>T , CM000681.2:g.40848635C>T GRCh38
NC_000019.9:g.41354540C>T , CM000681.1:g.41354540C>T GRCh37
NC_000019.8:g.46046380C>T NCBI36
NG_008377.1:g.6813G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000301141.10:c.472G>A MANE Select ENSP00000301141.4:p.Asp158Asn
ENST00000301141.9:c.472G>A ENSP00000301141.4:p.Asp158Asn
ENST00000596719.5:n.323G>A
ENST00000600495.1:c.*284G>A ENSP00000472905.1:n.*284G>A
ENST00000601627.1:c.120-43356C>T
ENST00000610301.1:c.472G>A ENSP00000477899.1:p.Asp158Asn
NM_000762.5:c.472G>A NP_000753.3:p.Asp158Asn
NM_000762.6:c.472G>A MANE Select NP_000753.3:p.Asp158Asn
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