Canonical Allele Identifier: CA2406578597
Gene: CYP2D6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42127662G= , CM000684.2:g.42127662G= GRCh38
NC_000022.10:g.42523664G= , CM000684.1:g.42523664G= GRCh37
NC_000022.9:g.40853608G= NCBI36
NG_008376.3:g.7330C=
NG_008376.4:g.8149C=

Transcript Alleles

HGVS Amino-acid change
ENST00000360124.10:c.784-28C= ENSP00000353241.6:n.784-28C=
ENST00000645361.2:c.986-28C= MANE Select ENSP00000496150.1:n.986-28C=
ENST00000359033.4:c.833-28C= ENSP00000351927.4:n.833-28C=
ENST00000360124.9:c.604-28C= ENSP00000353241.5:n.604-28C=
ENST00000360608.9:c.986-28C= ENSP00000353820.5:n.986-28C=
ENST00000389970.7:c.949C= ENSP00000374620.4:p.Pro317=
ENST00000488442.1:n.1710-28C=
NM_000106.5:c.986-28C= NP_000097.3:n.986-28C=
NM_001025161.2:c.833-28C= NP_001020332.2:n.833-28C=
XM_011529966.1:c.986-28C= XP_011528268.1:n.986-28C=
XM_011529967.1:c.986-28C= XP_011528269.1:n.986-28C=
XM_011529968.1:c.986-28C= XP_011528270.1:n.986-28C=
XM_011529969.1:c.842-28C= XP_011528271.1:n.842-28C=
XM_011529970.1:c.833-28C= XP_011528272.1:n.833-28C=
XM_011529971.1:c.842-28C= XP_011528273.1:n.842-28C=
XM_011529972.1:c.844-28C= XP_011528274.1:n.844-28C=
NM_000106.6:c.986-28C= MANE Select NP_000097.3:n.986-28C=
NM_001025161.3:c.833-28C= NP_001020332.2:n.833-28C=