Canonical Allele Identifier: CA2406578891
Gene: CYP2D6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42128075G= , CM000684.2:g.42128075G= GRCh38
NC_000022.10:g.42524077G= , CM000684.1:g.42524077G= GRCh37
NC_000022.9:g.40854021G= NCBI36
NG_008376.3:g.6917C=
NG_008376.4:g.7736C=

Transcript Alleles

HGVS Amino-acid change
ENST00000360124.10:c.690+99C= ENSP00000353241.6:n.690+99C=
ENST00000645361.2:c.844-92C= MANE Select ENSP00000496150.1:n.844-92C=
ENST00000359033.4:c.691-92C= ENSP00000351927.4:n.691-92C=
ENST00000360124.9:c.510+99C= ENSP00000353241.5:n.510+99C=
ENST00000360608.9:c.844-92C= ENSP00000353820.5:n.844-92C=
ENST00000389970.7:c.778-92C= ENSP00000374620.4:n.778-92C=
ENST00000488442.1:n.1568-92C=
NM_000106.5:c.844-92C= NP_000097.3:n.844-92C=
NM_001025161.2:c.691-92C= NP_001020332.2:n.691-92C=
XM_011529966.1:c.844-92C= XP_011528268.1:n.844-92C=
XM_011529967.1:c.844-92C= XP_011528269.1:n.844-92C=
XM_011529968.1:c.844-92C= XP_011528270.1:n.844-92C=
XM_011529969.1:c.700-92C= XP_011528271.1:n.700-92C=
XM_011529970.1:c.691-92C= XP_011528272.1:n.691-92C=
XM_011529971.1:c.700-92C= XP_011528273.1:n.700-92C=
XM_011529972.1:c.843+99C= XP_011528274.1:n.843+99C=
NM_000106.6:c.844-92C= MANE Select NP_000097.3:n.844-92C=
NM_001025161.3:c.691-92C= NP_001020332.2:n.691-92C=