Canonical Allele Identifier: CA915951433

Gene: CYP2D6

Linked Data

• ClinVar Variation Id: 828849
• ClinVar RCV Id: RCV001028760
• dbSNP Id: rs1602583762

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42129684T>C , CM000684.2:g.42129684T>C	GRCh38
NC_000022.10:g.42525686T>C , CM000684.1:g.42525686T>C	GRCh37
NC_000022.9:g.40855630T>C	NCBI36
NG_008376.3:g.5308A>G
NG_008376.4:g.6127A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.352+54A>G	ENSP00000353241.6:n.352+54A>G
ENST00000645361.2:c.352+54A>G MANE Select	ENSP00000496150.1:n.352+54A>G
ENST00000359033.4:c.352+54A>G	ENSP00000351927.4:n.352+54A>G
ENST00000360124.9:c.172+54A>G	ENSP00000353241.5:n.172+54A>G
ENST00000360608.9:c.352+54A>G	ENSP00000353820.5:n.352+54A>G
ENST00000389970.7:c.286+54A>G	ENSP00000374620.4:n.286+54A>G
ENST00000488442.1:n.1076+54A>G
NM_000106.5:c.352+54A>G	NP_000097.3:n.352+54A>G
NM_001025161.2:c.352+54A>G	NP_001020332.2:n.352+54A>G
XM_011529966.1:c.352+54A>G	XP_011528268.1:n.352+54A>G
XM_011529967.1:c.352+54A>G	XP_011528269.1:n.352+54A>G
XM_011529968.1:c.352+54A>G	XP_011528270.1:n.352+54A>G
XM_011529969.1:c.209+54A>G	XP_011528271.1:n.209+54A>G
XM_011529970.1:c.352+54A>G	XP_011528272.1:n.352+54A>G
XM_011529971.1:c.209+54A>G	XP_011528273.1:n.209+54A>G
XM_011529972.1:c.352+54A>G	XP_011528274.1:n.352+54A>G
NM_000106.6:c.352+54A>G MANE Select	NP_000097.3:n.352+54A>G
NM_001025161.3:c.352+54A>G	NP_001020332.2:n.352+54A>G