Canonical Allele Identifier: CA9452724
Gene: CYP2A6 HGNC NCBI

Linked Data

dbSNP Id: rs763405239
ExAC: 19:41351075 A / T
gnomAD v2: 19-41351075-A-T
gnomAD v4: 19-40845170-A-T
MyVariant Identifiers: chr19:g.41351075A>T (hg19) chr19:g.40845170A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40845170A>T , CM000681.2:g.40845170A>T GRCh38
NC_000019.9:g.41351075A>T , CM000681.1:g.41351075A>T GRCh37
NC_000019.8:g.46042915A>T NCBI36
NG_008377.1:g.10278T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000301141.10:c.1161+124T>A MANE Select ENSP00000301141.4:n.1161+124T>A
ENST00000301141.9:c.1161+124T>A ENSP00000301141.4:n.1161+124T>A
ENST00000596719.5:n.1136T>A
ENST00000601627.1:c.119+43755A>T
ENST00000610301.1:c.1161+124T>A ENSP00000477899.1:n.1161+124T>A
NM_000762.5:c.1161+124T>A NP_000753.3:n.1161+124T>A
NM_000762.6:c.1161+124T>A MANE Select NP_000753.3:n.1161+124T>A
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