Canonical Allele Identifier: CA308453664
Gene: CYP2A6 HGNC NCBI

Linked Data

dbSNP Id: rs932406508
gnomAD v2: 19-41351078-C-CT
gnomAD v3: 19-40845173-C-CT
gnomAD v4: 19-40845173-C-CT
MyVariant Identifiers: chr19:g.41351078_41351079insT (hg19) chr19:g.40845173_40845174insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40845179dup , CM000681.2:g.40845179dup GRCh38
NC_000019.9:g.41351084dup , CM000681.1:g.41351084dup GRCh37
NC_000019.8:g.46042924dup NCBI36
NG_008377.1:g.10274dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000301141.10:c.1161+120dup MANE Select ENSP00000301141.4:n.1161+120dup
ENST00000301141.9:c.1161+120dup ENSP00000301141.4:n.1161+120dup
ENST00000596719.5:n.1132dup
ENST00000601627.1:c.119+43764dup
ENST00000610301.1:c.1161+120dup ENSP00000477899.1:n.1161+120dup
NM_000762.5:c.1161+120dup NP_000753.3:n.1161+120dup
NM_000762.6:c.1161+120dup MANE Select NP_000753.3:n.1161+120dup
Search 100 bp 5'
Search 100 bp 3'