Canonical Allele Identifier: CA324672399
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs879622920

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42128945del , CM000684.2:g.42128945del GRCh38
NC_000022.10:g.42524947del , CM000684.1:g.42524947del GRCh37
NC_000022.9:g.40854891del NCBI36
NG_008376.3:g.6048del
NG_008376.4:g.6867del

Transcript Alleles

HGVS Amino-acid change
ENST00000645361.2:c.506del
ENST00000359033.4:c.353del
ENST00000360124.9:n.173del
ENST00000360608.9:c.506del
ENST00000389970.7:c.440del
ENST00000488442.1:n.1230del
NM_000106.5:c.506del
NM_001025161.2:c.353del
XM_011529966.1:c.506del
XM_011529967.1:c.506del
XM_011529968.1:c.506del
XM_011529969.1:c.363-1del XP_011528271.1:n.363-1del
XM_011529970.1:c.353del
XM_011529971.1:c.363-1del XP_011528273.1:n.363-1del
XM_011529972.1:c.506del
NM_000106.6:c.506del
NM_001025161.3:c.353del