Canonical Allele Identifier: CA411773306

Gene: CYP2D6

Linked Data

• MyVariant Identifiers: chr22:g.42524248C>G (hg19) ; chr22:g.42128246C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128246C>G , CM000684.2:g.42128246C>G	GRCh38
NC_000022.10:g.42524248C>G , CM000684.1:g.42524248C>G	GRCh37
NC_000022.9:g.40854192C>G	NCBI36
NG_008376.3:g.6746G>C
NG_008376.4:g.7565G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.618G>C	ENSP00000353241.6:p.Glu206Asp
ENST00000645361.2:c.771G>C MANE Select	ENSP00000496150.1:p.Glu257Asp
ENST00000359033.4:c.618G>C	ENSP00000351927.4:p.Glu206Asp
ENST00000360124.9:c.438G>C	ENSP00000353241.5:p.Glu146Asp
ENST00000360608.9:c.771G>C	ENSP00000353820.5:p.Glu257Asp
ENST00000389970.7:c.705G>C	ENSP00000374620.4:p.Glu235Asp
ENST00000488442.1:n.1495G>C
NM_000106.5:c.771G>C	NP_000097.3:p.Glu257Asp
NM_001025161.2:c.618G>C	NP_001020332.2:p.Glu206Asp
XM_011529966.1:c.771G>C	XP_011528268.1:p.Glu257Asp
XM_011529967.1:c.771G>C	XP_011528269.1:p.Glu257Asp
XM_011529968.1:c.771G>C	XP_011528270.1:p.Glu257Asp
XM_011529969.1:c.627G>C	XP_011528271.1:p.Glu209Asp
XM_011529970.1:c.618G>C	XP_011528272.1:p.Glu206Asp
XM_011529971.1:c.627G>C	XP_011528273.1:p.Glu209Asp
XM_011529972.1:c.771G>C	XP_011528274.1:p.Glu257Asp
NM_000106.6:c.771G>C MANE Select	NP_000097.3:p.Glu257Asp
NM_001025161.3:c.618G>C	NP_001020332.2:p.Glu206Asp