Canonical Allele Identifier: CA324664035
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs201339893

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42126138dup , CM000684.2:g.42126138dup GRCh38
NC_000022.10:g.42522140dup , CM000684.1:g.42522140dup GRCh37
NC_000022.9:g.40852084dup NCBI36
NG_008376.3:g.8854dup
NG_008376.4:g.9673dup

Transcript Alleles

HGVS Amino-acid Change
XM_011529966.1:c.1453-185dup XP_011528268.1:n.1453-185dup
XM_011529967.1:c.1453-185dup XP_011528269.1:n.1453-185dup
XM_011529968.1:c.1453-211dup XP_011528270.1:n.1453-211dup
XM_011529969.1:c.1309-185dup XP_011528271.1:n.1309-185dup
XM_011529970.1:c.1300-185dup XP_011528272.1:n.1300-185dup