Canonical Allele Identifier: CA1025921570

Gene: CYP2D6

Linked Data

• dbSNP Id: rs1931181578
• gnomAD v3: 22-42127812-GC-G
• gnomAD v4: 22-42127812-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42127816del , CM000684.2:g.42127816del	GRCh38
NC_000022.10:g.42523818del , CM000684.1:g.42523818del	GRCh37
NC_000022.9:g.40853762del	NCBI36
NG_008376.3:g.7179del
NG_008376.4:g.7998del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.783+29del	ENSP00000353241.6:n.783+29del
ENST00000645361.2:c.985+29del MANE Select	ENSP00000496150.1:n.985+29del
ENST00000359033.4:c.832+29del	ENSP00000351927.4:n.832+29del
ENST00000360124.9:c.603+29del	ENSP00000353241.5:n.603+29del
ENST00000360608.9:c.985+29del	ENSP00000353820.5:n.985+29del
ENST00000389970.7:c.920-4del	ENSP00000374620.4:n.920-4del
ENST00000488442.1:n.1709+29del
NM_000106.5:c.985+29del	NP_000097.3:n.985+29del
NM_001025161.2:c.832+29del	NP_001020332.2:n.832+29del
XM_011529966.1:c.985+29del	XP_011528268.1:n.985+29del
XM_011529967.1:c.985+29del	XP_011528269.1:n.985+29del
XM_011529968.1:c.985+29del	XP_011528270.1:n.985+29del
XM_011529969.1:c.841+29del	XP_011528271.1:n.841+29del
XM_011529970.1:c.832+29del	XP_011528272.1:n.832+29del
XM_011529971.1:c.841+29del	XP_011528273.1:n.841+29del
XM_011529972.1:c.844-179del	XP_011528274.1:n.844-179del
NM_000106.6:c.985+29del MANE Select	NP_000097.3:n.985+29del
NM_001025161.3:c.832+29del	NP_001020332.2:n.832+29del