Canonical Allele Identifier: CA411769891

Gene: CYP2D6

Linked Data

• MyVariant Identifiers: chr22:g.42522654C>A (hg19) ; chr22:g.42126652C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42126652C>A , CM000684.2:g.42126652C>A	GRCh38
NC_000022.10:g.42522654C>A , CM000684.1:g.42522654C>A	GRCh37
NC_000022.9:g.40852598C>A	NCBI36
NG_008376.3:g.8340G>T
NG_008376.4:g.9159G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.1214G>T	ENSP00000353241.6:n.1214G>T
ENST00000645361.2:c.1416G>T MANE Select	ENSP00000496150.1:p.Gln472His
ENST00000359033.4:c.1263G>T	ENSP00000351927.4:p.Gln421His
ENST00000360124.9:c.1034G>T	ENSP00000353241.5:n.1034G>T
ENST00000360608.9:c.1416G>T	ENSP00000353820.5:p.Gln472His
ENST00000389970.7:c.1407G>T	ENSP00000374620.4:p.Gln469His
ENST00000488442.1:n.2140G>T
NM_000106.5:c.1416G>T	NP_000097.3:p.Gln472His
NM_001025161.2:c.1263G>T	NP_001020332.2:p.Gln421His
XM_011529966.1:c.1416G>T	XP_011528268.1:p.Gln472His
XM_011529967.1:c.1416G>T	XP_011528269.1:p.Gln472His
XM_011529968.1:c.1416G>T	XP_011528270.1:p.Gln472His
XM_011529969.1:c.1272G>T	XP_011528271.1:p.Gln424His
XM_011529970.1:c.1263G>T	XP_011528272.1:p.Gln421His
XM_011529971.1:c.1272G>T	XP_011528273.1:p.Gln424His
NM_000106.6:c.1416G>T MANE Select	NP_000097.3:p.Gln472His
NM_001025161.3:c.1263G>T	NP_001020332.2:p.Gln421His