Canonical Allele Identifier: CA411773593

Gene: CYP2D6

Linked Data

• gnomAD v4: 22-42128338-C-T
• MyVariant Identifiers: chr22:g.42524340C>T (hg19) ; chr22:g.42128338C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128338C>T , CM000684.2:g.42128338C>T	GRCh38
NC_000022.10:g.42524340C>T , CM000684.1:g.42524340C>T	GRCh37
NC_000022.9:g.40854284C>T	NCBI36
NG_008376.3:g.6654G>A
NG_008376.4:g.7473G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.526G>A	ENSP00000353241.6:p.Val176Ile
ENST00000645361.2:c.679G>A MANE Select	ENSP00000496150.1:p.Val227Ile
ENST00000359033.4:c.526G>A	ENSP00000351927.4:p.Val176Ile
ENST00000360124.9:c.346G>A	ENSP00000353241.5:p.Val116Ile
ENST00000360608.9:c.679G>A	ENSP00000353820.5:p.Val227Ile
ENST00000389970.7:c.613G>A	ENSP00000374620.4:p.Val205Ile
ENST00000488442.1:n.1403G>A
NM_000106.5:c.679G>A	NP_000097.3:p.Val227Ile
NM_001025161.2:c.526G>A	NP_001020332.2:p.Val176Ile
XM_011529966.1:c.679G>A	XP_011528268.1:p.Val227Ile
XM_011529967.1:c.679G>A	XP_011528269.1:p.Val227Ile
XM_011529968.1:c.679G>A	XP_011528270.1:p.Val227Ile
XM_011529969.1:c.535G>A	XP_011528271.1:p.Val179Ile
XM_011529970.1:c.526G>A	XP_011528272.1:p.Val176Ile
XM_011529971.1:c.535G>A	XP_011528273.1:p.Val179Ile
XM_011529972.1:c.679G>A	XP_011528274.1:p.Val227Ile
NM_000106.6:c.679G>A MANE Select	NP_000097.3:p.Val227Ile
NM_001025161.3:c.526G>A	NP_001020332.2:p.Val176Ile