Canonical Allele Identifier: CA2406577775
Gene: CYP2D6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42126556G= , CM000684.2:g.42126556G= GRCh38
NC_000022.10:g.42522558G= , CM000684.1:g.42522558G= GRCh37
NC_000022.9:g.40852502G= NCBI36
NG_008376.3:g.8436C=
NG_008376.4:g.9255C=

Transcript Alleles

HGVS Amino-acid change
ENST00000360124.10:c.1310C= ENSP00000353241.6:n.1310C=
ENST00000645361.2:c.*18C= MANE Select ENSP00000496150.1:n.*18C=
ENST00000359033.4:c.*18C= ENSP00000351927.4:n.*18C=
ENST00000360124.9:c.1130C= ENSP00000353241.5:n.1130C=
ENST00000360608.9:c.*18C= ENSP00000353820.5:n.*18C=
ENST00000389970.7:c.*18C= ENSP00000374620.4:n.*18C=
ENST00000488442.1:n.2236C=
NM_000106.5:c.*18C= NP_000097.3:n.*18C=
NM_001025161.2:c.*18C= NP_001020332.2:n.*18C=
XM_011529966.1:c.1452+60C= XP_011528268.1:n.1452+60C=
XM_011529967.1:c.1452+60C= XP_011528269.1:n.1452+60C=
XM_011529968.1:c.1452+60C= XP_011528270.1:n.1452+60C=
XM_011529969.1:c.1308+60C= XP_011528271.1:n.1308+60C=
XM_011529970.1:c.1299+60C= XP_011528272.1:n.1299+60C=
XM_011529971.1:c.*18C= XP_011528273.1:n.*18C=
NM_000106.6:c.*18C= MANE Select NP_000097.3:n.*18C=
NM_001025161.3:c.*18C= NP_001020332.2:n.*18C=