Canonical Allele Identifier: CA753328648

Gene: CYP2D6

Linked Data

• dbSNP Id: rs1461547358
• gnomAD v3: 22-42128515-AGAG-A
• gnomAD v4: 22-42128515-AGAG-A
• MyVariant Identifiers: chr22:g.42128516_42128518del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128519_42128521del , CM000684.2:g.42128519_42128521del	GRCh38
NC_000022.10:g.42524521_42524523del , CM000684.1:g.42524521_42524523del	GRCh37
NC_000022.9:g.40854465_40854467del	NCBI36
NG_008376.3:g.6474_6476del
NG_008376.4:g.7293_7295del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.514-168_514-166del	ENSP00000353241.6:n.514-168_514-166del
ENST00000645361.2:c.667-168_667-166del MANE Select	ENSP00000496150.1:n.667-168_667-166del
ENST00000359033.4:c.514-168_514-166del	ENSP00000351927.4:n.514-168_514-166del
ENST00000360124.9:c.334-168_334-166del	ENSP00000353241.5:n.334-168_334-166del
ENST00000360608.9:c.667-168_667-166del	ENSP00000353820.5:n.667-168_667-166del
ENST00000389970.7:c.601-168_601-166del	ENSP00000374620.4:n.601-168_601-166del
ENST00000488442.1:n.1391-168_1391-166del
NM_000106.5:c.667-168_667-166del	NP_000097.3:n.667-168_667-166del
NM_001025161.2:c.514-168_514-166del	NP_001020332.2:n.514-168_514-166del
XM_011529966.1:c.667-168_667-166del	XP_011528268.1:n.667-168_667-166del
XM_011529967.1:c.667-168_667-166del	XP_011528269.1:n.667-168_667-166del
XM_011529968.1:c.667-168_667-166del	XP_011528270.1:n.667-168_667-166del
XM_011529969.1:c.523-168_523-166del	XP_011528271.1:n.523-168_523-166del
XM_011529970.1:c.514-168_514-166del	XP_011528272.1:n.514-168_514-166del
XM_011529971.1:c.523-168_523-166del	XP_011528273.1:n.523-168_523-166del
XM_011529972.1:c.667-168_667-166del	XP_011528274.1:n.667-168_667-166del
NM_000106.6:c.667-168_667-166del MANE Select	NP_000097.3:n.667-168_667-166del
NM_001025161.3:c.514-168_514-166del	NP_001020332.2:n.514-168_514-166del