Canonical Allele Identifier: CA9452774
Gene: CYP2A6 HGNC NCBI

Linked Data

dbSNP Id: rs756390851
ExAC: 19:41351218 C / T
gnomAD v2: 19-41351218-C-T
gnomAD v3: 19-40845313-C-T
gnomAD v4: 19-40845313-C-T
MyVariant Identifiers: chr19:g.41351218C>T (hg19) chr19:g.40845313C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40845313C>T , CM000681.2:g.40845313C>T GRCh38
NC_000019.9:g.41351218C>T , CM000681.1:g.41351218C>T GRCh37
NC_000019.8:g.46043058C>T NCBI36
NG_008377.1:g.10135G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000301141.10:c.1142G>A MANE Select ENSP00000301141.4:p.Arg381Gln
ENST00000301141.9:c.1142G>A ENSP00000301141.4:p.Arg381Gln
ENST00000596719.5:n.993G>A
ENST00000601627.1:c.119+43898C>T
ENST00000610301.1:c.1142G>A ENSP00000477899.1:p.Arg381Gln
NM_000762.5:c.1142G>A NP_000753.3:p.Arg381Gln
NM_000762.6:c.1142G>A MANE Select NP_000753.3:p.Arg381Gln
Search 100 bp 5'
Search 100 bp 3'