Canonical Allele Identifier: CA915951422

Gene: CYP2D6

Linked Data

• ClinVar Variation Id: 829663
• ClinVar RCV Id: RCV001029590
• dbSNP Id: rs1602580928

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42129206T>A , CM000684.2:g.42129206T>A	GRCh38
NC_000022.10:g.42525208T>A , CM000684.1:g.42525208T>A	GRCh37
NC_000022.9:g.40855152T>A	NCBI36
NG_008376.3:g.5786A>T
NG_008376.4:g.6605A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.353-262A>T	ENSP00000353241.6:n.353-262A>T
ENST00000645361.2:c.353-21A>T MANE Select	ENSP00000496150.1:n.353-21A>T
ENST00000359033.4:c.353-262A>T	ENSP00000351927.4:n.353-262A>T
ENST00000360124.9:c.173-262A>T	ENSP00000353241.5:n.173-262A>T
ENST00000360608.9:c.353-21A>T	ENSP00000353820.5:n.353-21A>T
ENST00000389970.7:c.287-21A>T	ENSP00000374620.4:n.287-21A>T
ENST00000488442.1:n.1077-21A>T
NM_000106.5:c.353-21A>T	NP_000097.3:n.353-21A>T
NM_001025161.2:c.353-262A>T	NP_001020332.2:n.353-262A>T
XM_011529966.1:c.353-21A>T	XP_011528268.1:n.353-21A>T
XM_011529967.1:c.353-21A>T	XP_011528269.1:n.353-21A>T
XM_011529968.1:c.353-21A>T	XP_011528270.1:n.353-21A>T
XM_011529969.1:c.210-21A>T	XP_011528271.1:n.210-21A>T
XM_011529970.1:c.353-262A>T	XP_011528272.1:n.353-262A>T
XM_011529971.1:c.210-21A>T	XP_011528273.1:n.210-21A>T
XM_011529972.1:c.353-21A>T	XP_011528274.1:n.353-21A>T
NM_000106.6:c.353-21A>T MANE Select	NP_000097.3:n.353-21A>T
NM_001025161.3:c.353-262A>T	NP_001020332.2:n.353-262A>T