Canonical Allele Identifier: CA411775738

Gene: CYP2D6

Linked Data

• dbSNP Id: rs2146943593
• MyVariant Identifiers: chr22:g.42526614C>A (hg19) ; chr22:g.42130612C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42130612C>A , CM000684.2:g.42130612C>A	GRCh38
NC_000022.10:g.42526614C>A , CM000684.1:g.42526614C>A	GRCh37
NC_000022.9:g.40856558C>A	NCBI36
NG_008376.3:g.4380G>T
NG_008376.4:g.5199G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.180G>T	ENSP00000353241.6:p.Gln60His
ENST00000645361.2:c.180G>T MANE Select	ENSP00000496150.1:p.Gln60His
ENST00000359033.4:c.180G>T	ENSP00000351927.4:p.Gln60His
ENST00000360608.9:c.180G>T	ENSP00000353820.5:p.Gln60His
ENST00000389970.7:c.114G>T	ENSP00000374620.4:p.Gln38His
ENST00000488442.1:n.202G>T
NM_000106.5:c.180G>T	NP_000097.3:p.Gln60His
NM_001025161.2:c.180G>T	NP_001020332.2:p.Gln60His
XM_011529966.1:c.180G>T	XP_011528268.1:p.Gln60His
XM_011529967.1:c.180G>T	XP_011528269.1:p.Gln60His
XM_011529968.1:c.180G>T	XP_011528270.1:p.Gln60His
XM_011529969.1:c.37+685G>T	XP_011528271.1:n.37+685G>T
XM_011529970.1:c.180G>T	XP_011528272.1:p.Gln60His
XM_011529971.1:c.37+685G>T	XP_011528273.1:n.37+685G>T
XM_011529972.1:c.180G>T	XP_011528274.1:p.Gln60His
XR_430455.2:n.252C>A
NM_000106.6:c.180G>T MANE Select	NP_000097.3:p.Gln60His
XR_002958749.1:n.199C>A
NM_001025161.3:c.180G>T	NP_001020332.2:p.Gln60His