Canonical Allele Identifier: CA995923325
Gene: CYP2A6 HGNC NCBI

Linked Data

dbSNP Id: rs1568513201
gnomAD v3: 19-40843718-G-C
gnomAD v4: 19-40843718-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40843718G>C , CM000681.2:g.40843718G>C GRCh38
NC_000019.9:g.41349623G>C , CM000681.1:g.41349623G>C GRCh37
NC_000019.8:g.46041463G>C NCBI36
NG_008377.1:g.11730C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000301141.10:c.*78C>G MANE Select ENSP00000301141.4:n.*78C>G
ENST00000301141.9:c.*78C>G ENSP00000301141.4:n.*78C>G
ENST00000599960.1:n.482C>G
ENST00000601627.1:c.119+42303G>C
NM_000762.5:c.*78C>G NP_000753.3:n.*78C>G
NM_000762.6:c.*78C>G MANE Select NP_000753.3:n.*78C>G
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