Canonical Allele Identifier: CA411772643

Gene: CYP2D6

Linked Data

• MyVariant Identifiers: chr22:g.42523921A>T (hg19) ; chr22:g.42127919A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42127919A>T , CM000684.2:g.42127919A>T	GRCh38
NC_000022.10:g.42523921A>T , CM000684.1:g.42523921A>T	GRCh37
NC_000022.9:g.40853865A>T	NCBI36
NG_008376.3:g.7073T>A
NG_008376.4:g.7892T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.706T>A	ENSP00000353241.6:p.Ser236Thr
ENST00000645361.2:c.908T>A MANE Select	ENSP00000496150.1:p.Phe303Tyr
ENST00000359033.4:c.755T>A	ENSP00000351927.4:p.Phe252Tyr
ENST00000360124.9:c.526T>A	ENSP00000353241.5:p.Ser176Thr
ENST00000360608.9:c.908T>A	ENSP00000353820.5:p.Phe303Tyr
ENST00000389970.7:c.842T>A	ENSP00000374620.4:p.Phe281Tyr
ENST00000488442.1:n.1632T>A
NM_000106.5:c.908T>A	NP_000097.3:p.Phe303Tyr
NM_001025161.2:c.755T>A	NP_001020332.2:p.Phe252Tyr
XM_011529966.1:c.908T>A	XP_011528268.1:p.Phe303Tyr
XM_011529967.1:c.908T>A	XP_011528269.1:p.Phe303Tyr
XM_011529968.1:c.908T>A	XP_011528270.1:p.Phe303Tyr
XM_011529969.1:c.764T>A	XP_011528271.1:p.Phe255Tyr
XM_011529970.1:c.755T>A	XP_011528272.1:p.Phe252Tyr
XM_011529971.1:c.764T>A	XP_011528273.1:p.Phe255Tyr
XM_011529972.1:c.843+255T>A	XP_011528274.1:n.843+255T>A
NM_000106.6:c.908T>A MANE Select	NP_000097.3:p.Phe303Tyr
NM_001025161.3:c.755T>A	NP_001020332.2:p.Phe252Tyr