Canonical Allele Identifier: CA2336176296
Gene: CYP2A6 HGNC NCBI

Linked Data

dbSNP Id: rs2083440981
gnomAD v3: 19-40843664-C-T
gnomAD v4: 19-40843664-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40843664C>T , CM000681.2:g.40843664C>T GRCh38
NC_000019.9:g.41349569C>T , CM000681.1:g.41349569C>T GRCh37
NC_000019.8:g.46041409C>T NCBI36
NG_008377.1:g.11784G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000301141.10:c.*132G>A MANE Select ENSP00000301141.4:n.*132G>A
ENST00000301141.9:c.*132G>A ENSP00000301141.4:n.*132G>A
ENST00000599960.1:n.536G>A
ENST00000601627.1:c.119+42249C>T
NM_000762.5:c.*132G>A NP_000753.3:n.*132G>A
NM_000762.6:c.*132G>A MANE Select NP_000753.3:n.*132G>A
Search 100 bp 5'
Search 100 bp 3'