Canonical Allele Identifier: CA995923231
Gene: CYP2A6 HGNC NCBI

Linked Data

gnomAD v3: 19-40843622-A-C
gnomAD v4: 19-40843622-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40843622A>C , CM000681.2:g.40843622A>C GRCh38
NC_000019.9:g.41349527A>C , CM000681.1:g.41349527A>C GRCh37
NC_000019.8:g.46041367A>C NCBI36
NG_008377.1:g.11826T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000301141.10:c.*174T>G MANE Select ENSP00000301141.4:n.*174T>G
ENST00000301141.9:c.*174T>G ENSP00000301141.4:n.*174T>G
ENST00000599960.1:n.578T>G
ENST00000601627.1:c.119+42207A>C
NM_000762.5:c.*174T>G NP_000753.3:n.*174T>G
NM_000762.6:c.*174T>G MANE Select NP_000753.3:n.*174T>G
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