Canonical Allele Identifier: CA308452559
Gene: CYP2A6 HGNC NCBI

Linked Data

dbSNP Id: rs28399474
gnomAD v3: 19-40843716-G-C
gnomAD v4: 19-40843716-G-C
MyVariant Identifiers: chr19:g.41349621G>C (hg19) chr19:g.40843716G>C (hg38)
JSON-LD

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000301141.10:c.*80C>G MANE Select ENSP00000301141.4:n.*80C>G
ENST00000301141.9:c.*80C>G ENSP00000301141.4:n.*80C>G
ENST00000599960.1:n.484C>G
ENST00000601627.1:c.119+42301G>C
NM_000762.5:c.*80C>G NP_000753.3:n.*80C>G
NM_000762.6:c.*80C>G MANE Select NP_000753.3:n.*80C>G
Search 100 bp 5'
Search 100 bp 3'