Canonical Allele Identifier: CA2406579516
Gene: CYP2D6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42128847G= , CM000684.2:g.42128847G= GRCh38
NC_000022.10:g.42524849G= , CM000684.1:g.42524849G= GRCh37
NC_000022.9:g.40854793G= NCBI36
NG_008376.3:g.6145C=
NG_008376.4:g.6964C=

Transcript Alleles

HGVS Amino-acid change
ENST00000360124.10:c.450C= ENSP00000353241.6:p.Arg150=
ENST00000645361.2:c.603C= MANE Select ENSP00000496150.1:p.Arg201=
ENST00000359033.4:c.450C= ENSP00000351927.4:p.Arg150=
ENST00000360124.9:c.270C= ENSP00000353241.5:p.Arg90=
ENST00000360608.9:c.603C= ENSP00000353820.5:p.Arg201=
ENST00000389970.7:c.537C= ENSP00000374620.4:p.Arg179=
ENST00000488442.1:n.1327C=
NM_000106.5:c.603C= NP_000097.3:p.Arg201=
NM_001025161.2:c.450C= NP_001020332.2:p.Arg150=
XM_011529966.1:c.603C= XP_011528268.1:p.Arg201=
XM_011529967.1:c.603C= XP_011528269.1:p.Arg201=
XM_011529968.1:c.603C= XP_011528270.1:p.Arg201=
XM_011529969.1:c.459C= XP_011528271.1:p.Arg153=
XM_011529970.1:c.450C= XP_011528272.1:p.Arg150=
XM_011529971.1:c.459C= XP_011528273.1:p.Arg153=
XM_011529972.1:c.603C= XP_011528274.1:p.Arg201=
NM_000106.6:c.603C= MANE Select NP_000097.3:p.Arg201=
NM_001025161.3:c.450C= NP_001020332.2:p.Arg150=