Canonical Allele Identifier: CA639828306

Gene: CYP2D6

Linked Data

• dbSNP Id: rs1483850901
• gnomAD v2: 22-42524980-TC-T
• gnomAD v3: 22-42128978-TC-T
• gnomAD v4: 22-42128978-TC-T
• MyVariant Identifiers: chr22:g.42524981del (hg19) ; chr22:g.42128979del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128982del , CM000684.2:g.42128982del	GRCh38
NC_000022.10:g.42524984del , CM000684.1:g.42524984del	GRCh37
NC_000022.9:g.40854928del	NCBI36
NG_008376.3:g.6013del
NG_008376.4:g.6832del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.353-35del	ENSP00000353241.6:n.353-35del
ENST00000645361.2:c.506-35del MANE Select	ENSP00000496150.1:n.506-35del
ENST00000359033.4:c.353-35del	ENSP00000351927.4:n.353-35del
ENST00000360124.9:c.173-35del	ENSP00000353241.5:n.173-35del
ENST00000360608.9:c.506-35del	ENSP00000353820.5:n.506-35del
ENST00000389970.7:c.440-35del	ENSP00000374620.4:n.440-35del
ENST00000488442.1:n.1230-35del
NM_000106.5:c.506-35del	NP_000097.3:n.506-35del
NM_001025161.2:c.353-35del	NP_001020332.2:n.353-35del
XM_011529966.1:c.506-35del	XP_011528268.1:n.506-35del
XM_011529967.1:c.506-35del	XP_011528269.1:n.506-35del
XM_011529968.1:c.506-35del	XP_011528270.1:n.506-35del
XM_011529969.1:c.363-36del	XP_011528271.1:n.363-36del
XM_011529970.1:c.353-35del	XP_011528272.1:n.353-35del
XM_011529971.1:c.363-36del	XP_011528273.1:n.363-36del
XM_011529972.1:c.506-35del	XP_011528274.1:n.506-35del
NM_000106.6:c.506-35del MANE Select	NP_000097.3:n.506-35del
NM_001025161.3:c.353-35del	NP_001020332.2:n.353-35del