Canonical Allele Identifier: CA995923385
Gene: CYP2A6 HGNC NCBI

Linked Data

dbSNP Id: rs2083441775
gnomAD v3: 19-40843771-A-G
gnomAD v4: 19-40843771-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40843771A>G , CM000681.2:g.40843771A>G GRCh38
NC_000019.9:g.41349676A>G , CM000681.1:g.41349676A>G GRCh37
NC_000019.8:g.46041516A>G NCBI36
NG_008377.1:g.11677T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000301141.10:c.*25T>C MANE Select ENSP00000301141.4:n.*25T>C
ENST00000301141.9:c.*25T>C ENSP00000301141.4:n.*25T>C
ENST00000599960.1:n.429T>C
ENST00000601627.1:c.119+42356A>G
NM_000762.5:c.*25T>C NP_000753.3:n.*25T>C
NM_000762.6:c.*25T>C MANE Select NP_000753.3:n.*25T>C
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