Canonical Allele Identifier: CA126952
Gene: CYP2D6 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 16889
dbSNP Id: rs3892097

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42128945C>T , CM000684.2:g.42128945C>T GRCh38
NC_000022.9:g.40854891C>T NCBI36
NC_000022.10:g.42524947C>T , CM000684.1:g.42524947C>T GRCh37
NG_008376.3:g.6047G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000359033.4:c.353-1G>A ENSP00000351927.4:p.=
ENST00000360124.9:n.173-1G>A ENSP00000353241.5:p.=
ENST00000360608.9:c.506-1G>A ENSP00000353820.5:p.=
ENST00000389970.7:c.440-1G>A ENSP00000374620.4:p.=
ENST00000488442.1:n.1230-1G>A
NM_000106.5:c.506-1G>A VV NP_000097.3:p.=
NM_001025161.2:c.353-1G>A VV NP_001020332.2:p.=
XM_011529966.1:c.506-1G>A XP_011528268.1:p.=
XM_011529967.1:c.506-1G>A XP_011528269.1:p.=
XM_011529968.1:c.506-1G>A XP_011528270.1:p.=
XM_011529969.1:c.363-2G>A XP_011528271.1:p.=
XM_011529970.1:c.353-1G>A XP_011528272.1:p.=
XM_011529971.1:c.363-2G>A XP_011528273.1:p.=
XM_011529972.1:c.506-1G>A XP_011528274.1:p.=