Canonical Allele Identifier: CA995924009
Gene: CYP2A6 HGNC NCBI

Linked Data

dbSNP Id: rs2083448519
gnomAD v3: 19-40844998-G-GA
gnomAD v4: 19-40844998-G-GA
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40844999dup , CM000681.2:g.40844999dup GRCh38
NC_000019.9:g.41350904dup , CM000681.1:g.41350904dup GRCh37
NC_000019.8:g.46042744dup NCBI36
NG_008377.1:g.10449dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000301141.10:c.1162-227dup MANE Select ENSP00000301141.4:n.1162-227dup
ENST00000301141.9:c.1162-227dup ENSP00000301141.4:n.1162-227dup
ENST00000596719.5:n.1307dup
ENST00000601627.1:c.119+43584dup
ENST00000610301.1:c.1162-227dup ENSP00000477899.1:n.1162-227dup
NM_000762.5:c.1162-227dup NP_000753.3:n.1162-227dup
NM_000762.6:c.1162-227dup MANE Select NP_000753.3:n.1162-227dup
Search 100 bp 5'
Search 100 bp 3'