Canonical Allele Identifier: CA2406579528
Gene: CYP2D6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42128860T= , CM000684.2:g.42128860T= GRCh38
NC_000022.10:g.42524862T= , CM000684.1:g.42524862T= GRCh37
NC_000022.9:g.40854806T= NCBI36
NG_008376.3:g.6132A=
NG_008376.4:g.6951A=

Transcript Alleles

HGVS Amino-acid change
ENST00000360124.10:c.437A= ENSP00000353241.6:p.Tyr146=
ENST00000645361.2:c.590A= MANE Select ENSP00000496150.1:p.Tyr197=
ENST00000359033.4:c.437A= ENSP00000351927.4:p.Tyr146=
ENST00000360124.9:c.257A= ENSP00000353241.5:p.Tyr86=
ENST00000360608.9:c.590A= ENSP00000353820.5:p.Tyr197=
ENST00000389970.7:c.524A= ENSP00000374620.4:p.Tyr175=
ENST00000488442.1:n.1314A=
NM_000106.5:c.590A= NP_000097.3:p.Tyr197=
NM_001025161.2:c.437A= NP_001020332.2:p.Tyr146=
XM_011529966.1:c.590A= XP_011528268.1:p.Tyr197=
XM_011529967.1:c.590A= XP_011528269.1:p.Tyr197=
XM_011529968.1:c.590A= XP_011528270.1:p.Tyr197=
XM_011529969.1:c.446A= XP_011528271.1:p.Tyr149=
XM_011529970.1:c.437A= XP_011528272.1:p.Tyr146=
XM_011529971.1:c.446A= XP_011528273.1:p.Tyr149=
XM_011529972.1:c.590A= XP_011528274.1:p.Tyr197=
NM_000106.6:c.590A= MANE Select NP_000097.3:p.Tyr197=
NM_001025161.3:c.437A= NP_001020332.2:p.Tyr146=