Canonical Allele Identifier: CA2585203646
Gene: CYP2A6 HGNC NCBI

Linked Data

gnomAD v4: 19-40843620-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40843620G>T , CM000681.2:g.40843620G>T GRCh38
NC_000019.9:g.41349525G>T , CM000681.1:g.41349525G>T GRCh37
NC_000019.8:g.46041365G>T NCBI36
NG_008377.1:g.11828C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000301141.10:c.*176C>A MANE Select ENSP00000301141.4:n.*176C>A
ENST00000301141.9:c.*176C>A ENSP00000301141.4:n.*176C>A
ENST00000599960.1:n.580C>A
ENST00000601627.1:c.119+42205G>T
NM_000762.5:c.*176C>A NP_000753.3:n.*176C>A
NM_000762.6:c.*176C>A MANE Select NP_000753.3:n.*176C>A
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