Canonical Allele Identifier: CA2406577771
Gene: CYP2D6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42126551G= , CM000684.2:g.42126551G= GRCh38
NC_000022.10:g.42522553G= , CM000684.1:g.42522553G= GRCh37
NC_000022.9:g.40852497G= NCBI36
NG_008376.3:g.8441C=
NG_008376.4:g.9260C=

Transcript Alleles

HGVS Amino-acid change
ENST00000360124.10:c.1315C= ENSP00000353241.6:n.1315C=
ENST00000645361.2:c.*23C= MANE Select ENSP00000496150.1:n.*23C=
ENST00000360124.9:c.1135C= ENSP00000353241.5:n.1135C=
ENST00000360608.9:c.*23C= ENSP00000353820.5:n.*23C=
ENST00000389970.7:c.*23C= ENSP00000374620.4:n.*23C=
ENST00000488442.1:n.2241C=
NM_000106.5:c.*23C= NP_000097.3:n.*23C=
NM_001025161.2:c.*23C= NP_001020332.2:n.*23C=
XM_011529966.1:c.1452+65C= XP_011528268.1:n.1452+65C=
XM_011529967.1:c.1452+65C= XP_011528269.1:n.1452+65C=
XM_011529968.1:c.1452+65C= XP_011528270.1:n.1452+65C=
XM_011529969.1:c.1308+65C= XP_011528271.1:n.1308+65C=
XM_011529970.1:c.1299+65C= XP_011528272.1:n.1299+65C=
XM_011529971.1:c.*23C= XP_011528273.1:n.*23C=
NM_000106.6:c.*23C= MANE Select NP_000097.3:n.*23C=
NM_001025161.3:c.*23C= NP_001020332.2:n.*23C=