Canonical Allele Identifier: CA411773941

Gene: CYP2D6

Linked Data

• dbSNP Id: rs948982668
• gnomAD v4: 22-42128863-T-A
• MyVariant Identifiers: chr22:g.42524865T>A (hg19) ; chr22:g.42128863T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128863T>A , CM000684.2:g.42128863T>A	GRCh38
NC_000022.10:g.42524865T>A , CM000684.1:g.42524865T>A	GRCh37
NC_000022.9:g.40854809T>A	NCBI36
NG_008376.3:g.6129A>T
NG_008376.4:g.6948A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.434A>T	ENSP00000353241.6:p.Glu145Val
ENST00000645361.2:c.587A>T MANE Select	ENSP00000496150.1:p.Glu196Val
ENST00000359033.4:c.434A>T	ENSP00000351927.4:p.Glu145Val
ENST00000360124.9:c.254A>T	ENSP00000353241.5:p.Glu85Val
ENST00000360608.9:c.587A>T	ENSP00000353820.5:p.Glu196Val
ENST00000389970.7:c.521A>T	ENSP00000374620.4:p.Glu174Val
ENST00000488442.1:n.1311A>T
NM_000106.5:c.587A>T	NP_000097.3:p.Glu196Val
NM_001025161.2:c.434A>T	NP_001020332.2:p.Glu145Val
XM_011529966.1:c.587A>T	XP_011528268.1:p.Glu196Val
XM_011529967.1:c.587A>T	XP_011528269.1:p.Glu196Val
XM_011529968.1:c.587A>T	XP_011528270.1:p.Glu196Val
XM_011529969.1:c.443A>T	XP_011528271.1:p.Glu148Val
XM_011529970.1:c.434A>T	XP_011528272.1:p.Glu145Val
XM_011529971.1:c.443A>T	XP_011528273.1:p.Glu148Val
XM_011529972.1:c.587A>T	XP_011528274.1:p.Glu196Val
NM_000106.6:c.587A>T MANE Select	NP_000097.3:p.Glu196Val
NM_001025161.3:c.434A>T	NP_001020332.2:p.Glu145Val