Canonical Allele Identifier: CA920373718
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs1569025100

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42128964del , CM000684.2:g.42128964del GRCh38
NC_000022.10:g.42524966del , CM000684.1:g.42524966del GRCh37
NC_000022.9:g.40854910del NCBI36
NG_008376.3:g.6030del
NG_008376.4:g.6849del

Transcript Alleles

HGVS Amino-acid change
ENST00000645361.2:c.506-18del MANE Select ENSP00000496150.1:n.506-18del
ENST00000359033.4:c.353-18del ENSP00000351927.4:n.353-18del
ENST00000360124.9:n.173-18del ENSP00000353241.5:n.173-18del
ENST00000360608.9:c.506-18del ENSP00000353820.5:n.506-18del
ENST00000389970.7:c.440-18del ENSP00000374620.4:n.440-18del
ENST00000488442.1:n.1230-18del
NM_000106.5:c.506-18del NP_000097.3:n.506-18del
NM_001025161.2:c.353-18del NP_001020332.2:n.353-18del
XM_011529966.1:c.506-18del XP_011528268.1:n.506-18del
XM_011529967.1:c.506-18del XP_011528269.1:n.506-18del
XM_011529968.1:c.506-18del XP_011528270.1:n.506-18del
XM_011529969.1:c.363-19del XP_011528271.1:n.363-19del
XM_011529970.1:c.353-18del XP_011528272.1:n.353-18del
XM_011529971.1:c.363-19del XP_011528273.1:n.363-19del
XM_011529972.1:c.506-18del XP_011528274.1:n.506-18del
NM_000106.6:c.506-18del MANE Select NP_000097.3:n.506-18del
NM_001025161.3:c.353-18del NP_001020332.2:n.353-18del