Canonical Allele Identifier: CA995923322
Gene: CYP2A6 HGNC NCBI

Linked Data

dbSNP Id: rs28399474
gnomAD v3: 19-40843716-G-A
gnomAD v4: 19-40843716-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40843716G>A , CM000681.2:g.40843716G>A GRCh38
NC_000019.9:g.41349621G>A , CM000681.1:g.41349621G>A GRCh37
NC_000019.8:g.46041461G>A NCBI36
NG_008377.1:g.11732C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000301141.10:c.*80C>T MANE Select ENSP00000301141.4:n.*80C>T
ENST00000301141.9:c.*80C>T ENSP00000301141.4:n.*80C>T
ENST00000599960.1:n.484C>T
ENST00000601627.1:c.119+42301G>A
NM_000762.5:c.*80C>T NP_000753.3:n.*80C>T
NM_000762.6:c.*80C>T MANE Select NP_000753.3:n.*80C>T
Search 100 bp 5'
Search 100 bp 3'