Canonical Allele Identifier: CA882275988
Gene: CYP2A6 HGNC NCBI

Linked Data

dbSNP Id: rs1250237402
gnomAD v3: 19-40843766-C-G
gnomAD v4: 19-40843766-C-G
MyVariant Identifiers: chr19:g.41349671C>G (hg19) chr19:g.40843766C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40843766C>G , CM000681.2:g.40843766C>G GRCh38
NC_000019.9:g.41349671C>G , CM000681.1:g.41349671C>G GRCh37
NC_000019.8:g.46041511C>G NCBI36
NG_008377.1:g.11682G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000301141.10:c.*30G>C MANE Select ENSP00000301141.4:n.*30G>C
ENST00000301141.9:c.*30G>C ENSP00000301141.4:n.*30G>C
ENST00000599960.1:n.434G>C
ENST00000601627.1:c.119+42351C>G
NM_000762.5:c.*30G>C NP_000753.3:n.*30G>C
NM_000762.6:c.*30G>C MANE Select NP_000753.3:n.*30G>C
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