Canonical Allele Identifier: CA753331408

Gene: CYP2D6

Linked Data

• dbSNP Id: rs1439163480
• gnomAD v3: 22-42130489-C-T
• gnomAD v4: 22-42130489-C-T
• MyVariant Identifiers: chr22:g.42130489C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42130489C>T , CM000684.2:g.42130489C>T	GRCh38
NC_000022.10:g.42526491C>T , CM000684.1:g.42526491C>T	GRCh37
NC_000022.9:g.40856435C>T	NCBI36
NG_008376.3:g.4503G>A
NG_008376.4:g.5322G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.180+123G>A	ENSP00000353241.6:n.180+123G>A
ENST00000645361.2:c.180+123G>A MANE Select	ENSP00000496150.1:n.180+123G>A
ENST00000359033.4:c.180+123G>A	ENSP00000351927.4:n.180+123G>A
ENST00000360608.9:c.180+123G>A	ENSP00000353820.5:n.180+123G>A
ENST00000389970.7:c.114+123G>A	ENSP00000374620.4:n.114+123G>A
ENST00000488442.1:n.325G>A
NM_000106.5:c.180+123G>A	NP_000097.3:n.180+123G>A
NM_001025161.2:c.180+123G>A	NP_001020332.2:n.180+123G>A
XM_011529966.1:c.180+123G>A	XP_011528268.1:n.180+123G>A
XM_011529967.1:c.180+123G>A	XP_011528269.1:n.180+123G>A
XM_011529968.1:c.180+123G>A	XP_011528270.1:n.180+123G>A
XM_011529969.1:c.38-580G>A	XP_011528271.1:n.38-580G>A
XM_011529970.1:c.180+123G>A	XP_011528272.1:n.180+123G>A
XM_011529971.1:c.38-580G>A	XP_011528273.1:n.38-580G>A
XM_011529972.1:c.180+123G>A	XP_011528274.1:n.180+123G>A
XR_430455.2:n.207-78C>T
NM_000106.6:c.180+123G>A MANE Select	NP_000097.3:n.180+123G>A
XR_002958749.1:n.154-78C>T
NM_001025161.3:c.180+123G>A	NP_001020332.2:n.180+123G>A