Canonical Allele Identifier: CA514800262

Gene: CYP2D6

Linked Data

• gnomAD v4: 22-42128183-C-T
• MyVariant Identifiers: chr22:g.42524185C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128183C>T , CM000684.2:g.42128183C>T	GRCh38
NC_000022.10:g.42524185C>T , CM000684.1:g.42524185C>T	GRCh37
NC_000022.9:g.40854129C>T	NCBI36
NG_008376.3:g.6809G>A
NG_008376.4:g.7628G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.681G>A	ENSP00000353241.6:p.Glu227=
ENST00000645361.2:c.834G>A MANE Select	ENSP00000496150.1:p.Glu278=
ENST00000359033.4:c.681G>A	ENSP00000351927.4:p.Glu227=
ENST00000360124.9:c.501G>A	ENSP00000353241.5:p.Glu167=
ENST00000360608.9:c.834G>A	ENSP00000353820.5:p.Glu278=
ENST00000389970.7:c.768G>A	ENSP00000374620.4:p.Glu256=
ENST00000488442.1:n.1558G>A
NM_000106.5:c.834G>A	NP_000097.3:p.Glu278=
NM_001025161.2:c.681G>A	NP_001020332.2:p.Glu227=
XM_011529966.1:c.834G>A	XP_011528268.1:p.Glu278=
XM_011529967.1:c.834G>A	XP_011528269.1:p.Glu278=
XM_011529968.1:c.834G>A	XP_011528270.1:p.Glu278=
XM_011529969.1:c.690G>A	XP_011528271.1:p.Glu230=
XM_011529970.1:c.681G>A	XP_011528272.1:p.Glu227=
XM_011529971.1:c.690G>A	XP_011528273.1:p.Glu230=
XM_011529972.1:c.834G>A	XP_011528274.1:p.Glu278=
NM_000106.6:c.834G>A MANE Select	NP_000097.3:p.Glu278=
NM_001025161.3:c.681G>A	NP_001020332.2:p.Glu227=