Canonical Allele Identifier: CA411772273

Gene: CYP2D6

Linked Data

• dbSNP Id: rs747917111
• MyVariant Identifiers: chr22:g.42523806C>T (hg19) ; chr22:g.42127804C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42127804C>T , CM000684.2:g.42127804C>T	GRCh38
NC_000022.10:g.42523806C>T , CM000684.1:g.42523806C>T	GRCh37
NC_000022.9:g.40853750C>T	NCBI36
NG_008376.3:g.7188G>A
NG_008376.4:g.8007G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.783+38G>A	ENSP00000353241.6:n.783+38G>A
ENST00000645361.2:c.985+38G>A MANE Select	ENSP00000496150.1:n.985+38G>A
ENST00000359033.4:c.832+38G>A	ENSP00000351927.4:n.832+38G>A
ENST00000360124.9:c.603+38G>A	ENSP00000353241.5:n.603+38G>A
ENST00000360608.9:c.985+38G>A	ENSP00000353820.5:n.985+38G>A
ENST00000389970.7:c.925G>A	ENSP00000374620.4:p.Gly309Arg
ENST00000488442.1:n.1709+38G>A
NM_000106.5:c.985+38G>A	NP_000097.3:n.985+38G>A
NM_001025161.2:c.832+38G>A	NP_001020332.2:n.832+38G>A
XM_011529966.1:c.985+38G>A	XP_011528268.1:n.985+38G>A
XM_011529967.1:c.985+38G>A	XP_011528269.1:n.985+38G>A
XM_011529968.1:c.985+38G>A	XP_011528270.1:n.985+38G>A
XM_011529969.1:c.841+38G>A	XP_011528271.1:n.841+38G>A
XM_011529970.1:c.832+38G>A	XP_011528272.1:n.832+38G>A
XM_011529971.1:c.841+38G>A	XP_011528273.1:n.841+38G>A
XM_011529972.1:c.844-170G>A	XP_011528274.1:n.844-170G>A
NM_000106.6:c.985+38G>A MANE Select	NP_000097.3:n.985+38G>A
NM_001025161.3:c.832+38G>A	NP_001020332.2:n.832+38G>A