Canonical Allele Identifier: CA10265355

Gene: CYP2D6

Linked Data - Expert Curation

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42130668C>T , CM000684.2:g.42130668C>T	GRCh38
NC_000022.10:g.42526670C>T , CM000684.1:g.42526670C>T	GRCh37
NC_000022.9:g.40856614C>T	NCBI36
NG_008376.3:g.4324G>A
NG_008376.4:g.5143G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.124G>A	ENSP00000353241.6:p.Gly42Arg
ENST00000645361.2:c.124G>A MANE Select	ENSP00000496150.1:p.Gly42Arg
ENST00000359033.4:c.124G>A	ENSP00000351927.4:p.Gly42Arg
ENST00000360608.9:c.124G>A	ENSP00000353820.5:p.Gly42Arg
ENST00000389970.7:c.58G>A	ENSP00000374620.4:p.Gly20Arg
ENST00000488442.1:n.146G>A
NM_000106.5:c.124G>A	NP_000097.3:p.Gly42Arg
NM_001025161.2:c.124G>A	NP_001020332.2:p.Gly42Arg
XM_011529966.1:c.124G>A	XP_011528268.1:p.Gly42Arg
XM_011529967.1:c.124G>A	XP_011528269.1:p.Gly42Arg
XM_011529968.1:c.124G>A	XP_011528270.1:p.Gly42Arg
XM_011529969.1:c.37+629G>A	XP_011528271.1:n.37+629G>A
XM_011529970.1:c.124G>A	XP_011528272.1:p.Gly42Arg
XM_011529971.1:c.37+629G>A	XP_011528273.1:n.37+629G>A
XM_011529972.1:c.124G>A	XP_011528274.1:p.Gly42Arg
XR_430455.2:n.308C>T
NM_000106.6:c.124G>A MANE Select	NP_000097.3:p.Gly42Arg
XR_002958749.1:n.255C>T
NM_001025161.3:c.124G>A	NP_001020332.2:p.Gly42Arg