Canonical Allele Identifier: CA2406579527
Gene: CYP2D6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42128859G= , CM000684.2:g.42128859G= GRCh38
NC_000022.10:g.42524861G= , CM000684.1:g.42524861G= GRCh37
NC_000022.9:g.40854805G= NCBI36
NG_008376.3:g.6133C=
NG_008376.4:g.6952C=

Transcript Alleles

HGVS Amino-acid change
ENST00000360124.10:c.438C= ENSP00000353241.6:p.Tyr146=
ENST00000645361.2:c.591C= MANE Select ENSP00000496150.1:p.Tyr197=
ENST00000359033.4:c.438C= ENSP00000351927.4:p.Tyr146=
ENST00000360124.9:c.258C= ENSP00000353241.5:p.Tyr86=
ENST00000360608.9:c.591C= ENSP00000353820.5:p.Tyr197=
ENST00000389970.7:c.525C= ENSP00000374620.4:p.Tyr175=
ENST00000488442.1:n.1315C=
NM_000106.5:c.591C= NP_000097.3:p.Tyr197=
NM_001025161.2:c.438C= NP_001020332.2:p.Tyr146=
XM_011529966.1:c.591C= XP_011528268.1:p.Tyr197=
XM_011529967.1:c.591C= XP_011528269.1:p.Tyr197=
XM_011529968.1:c.591C= XP_011528270.1:p.Tyr197=
XM_011529969.1:c.447C= XP_011528271.1:p.Tyr149=
XM_011529970.1:c.438C= XP_011528272.1:p.Tyr146=
XM_011529971.1:c.447C= XP_011528273.1:p.Tyr149=
XM_011529972.1:c.591C= XP_011528274.1:p.Tyr197=
NM_000106.6:c.591C= MANE Select NP_000097.3:p.Tyr197=
NM_001025161.3:c.438C= NP_001020332.2:p.Tyr146=