Canonical Allele Identifier: CA411771855

Gene: CYP2D6

Linked Data

• dbSNP Id: rs758920219
• MyVariant Identifiers: chr22:g.42523599C>A (hg19) ; chr22:g.42127597C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42127597C>A , CM000684.2:g.42127597C>A	GRCh38
NC_000022.10:g.42523599C>A , CM000684.1:g.42523599C>A	GRCh37
NC_000022.9:g.40853543C>A	NCBI36
NG_008376.3:g.7395G>T
NG_008376.4:g.8214G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.821G>T	ENSP00000353241.6:n.821G>T
ENST00000645361.2:c.1023G>T MANE Select	ENSP00000496150.1:p.Gln341His
ENST00000359033.4:c.870G>T	ENSP00000351927.4:p.Gln290His
ENST00000360124.9:c.641G>T	ENSP00000353241.5:n.641G>T
ENST00000360608.9:c.1023G>T	ENSP00000353820.5:p.Gln341His
ENST00000389970.7:c.1014G>T	ENSP00000374620.4:p.Gln338His
ENST00000488442.1:n.1747G>T
NM_000106.5:c.1023G>T	NP_000097.3:p.Gln341His
NM_001025161.2:c.870G>T	NP_001020332.2:p.Gln290His
XM_011529966.1:c.1023G>T	XP_011528268.1:p.Gln341His
XM_011529967.1:c.1023G>T	XP_011528269.1:p.Gln341His
XM_011529968.1:c.1023G>T	XP_011528270.1:p.Gln341His
XM_011529969.1:c.879G>T	XP_011528271.1:p.Gln293His
XM_011529970.1:c.870G>T	XP_011528272.1:p.Gln290His
XM_011529971.1:c.879G>T	XP_011528273.1:p.Gln293His
XM_011529972.1:c.*8G>T	XP_011528274.1:n.*8G>T
NM_000106.6:c.1023G>T MANE Select	NP_000097.3:p.Gln341His
NM_001025161.3:c.870G>T	NP_001020332.2:p.Gln290His