Canonical Allele Identifier: CA2406577772
Gene: CYP2D6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42126552G= , CM000684.2:g.42126552G= GRCh38
NC_000022.10:g.42522554G= , CM000684.1:g.42522554G= GRCh37
NC_000022.9:g.40852498G= NCBI36
NG_008376.3:g.8440C=
NG_008376.4:g.9259C=

Transcript Alleles

HGVS Amino-acid change
ENST00000360124.10:c.1314C= ENSP00000353241.6:n.1314C=
ENST00000645361.2:c.*22C= MANE Select ENSP00000496150.1:n.*22C=
ENST00000360124.9:c.1134C= ENSP00000353241.5:n.1134C=
ENST00000360608.9:c.*22C= ENSP00000353820.5:n.*22C=
ENST00000389970.7:c.*22C= ENSP00000374620.4:n.*22C=
ENST00000488442.1:n.2240C=
NM_000106.5:c.*22C= NP_000097.3:n.*22C=
NM_001025161.2:c.*22C= NP_001020332.2:n.*22C=
XM_011529966.1:c.1452+64C= XP_011528268.1:n.1452+64C=
XM_011529967.1:c.1452+64C= XP_011528269.1:n.1452+64C=
XM_011529968.1:c.1452+64C= XP_011528270.1:n.1452+64C=
XM_011529969.1:c.1308+64C= XP_011528271.1:n.1308+64C=
XM_011529970.1:c.1299+64C= XP_011528272.1:n.1299+64C=
XM_011529971.1:c.*22C= XP_011528273.1:n.*22C=
NM_000106.6:c.*22C= MANE Select NP_000097.3:n.*22C=
NM_001025161.3:c.*22C= NP_001020332.2:n.*22C=