Canonical Allele Identifier: CA882275904
Gene: CYP2A6 HGNC NCBI

Linked Data

dbSNP Id: rs111419867
gnomAD v3: 19-40843613-C-A
gnomAD v4: 19-40843613-C-A
MyVariant Identifiers: chr19:g.41349518C>A (hg19) chr19:g.40843613C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40843613C>A , CM000681.2:g.40843613C>A GRCh38
NC_000019.9:g.41349518C>A , CM000681.1:g.41349518C>A GRCh37
NC_000019.8:g.46041358C>A NCBI36
NG_008377.1:g.11835G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000301141.10:c.*183G>T MANE Select ENSP00000301141.4:n.*183G>T
ENST00000301141.9:c.*183G>T ENSP00000301141.4:n.*183G>T
ENST00000599960.1:n.587G>T
ENST00000601627.1:c.119+42198C>A
NM_000762.5:c.*183G>T NP_000753.3:n.*183G>T
NM_000762.6:c.*183G>T MANE Select NP_000753.3:n.*183G>T
Search 100 bp 5'
Search 100 bp 3'