Canonical Allele Identifier: CA324670652

Gene: CYP2D6

Linked Data

• dbSNP Id: rs888621701
• gnomAD v2: 22-42524076-C-T
• gnomAD v3: 22-42128074-C-T
• gnomAD v4: 22-42128074-C-T
• MyVariant Identifiers: chr22:g.42524076C>T (hg19) ; chr22:g.42128074C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128074C>T , CM000684.2:g.42128074C>T	GRCh38
NC_000022.10:g.42524076C>T , CM000684.1:g.42524076C>T	GRCh37
NC_000022.9:g.40854020C>T	NCBI36
NG_008376.3:g.6918G>A
NG_008376.4:g.7737G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.690+100G>A	ENSP00000353241.6:n.690+100G>A
ENST00000645361.2:c.844-91G>A MANE Select	ENSP00000496150.1:n.844-91G>A
ENST00000359033.4:c.691-91G>A	ENSP00000351927.4:n.691-91G>A
ENST00000360124.9:c.510+100G>A	ENSP00000353241.5:n.510+100G>A
ENST00000360608.9:c.844-91G>A	ENSP00000353820.5:n.844-91G>A
ENST00000389970.7:c.778-91G>A	ENSP00000374620.4:n.778-91G>A
ENST00000488442.1:n.1568-91G>A
NM_000106.5:c.844-91G>A	NP_000097.3:n.844-91G>A
NM_001025161.2:c.691-91G>A	NP_001020332.2:n.691-91G>A
XM_011529966.1:c.844-91G>A	XP_011528268.1:n.844-91G>A
XM_011529967.1:c.844-91G>A	XP_011528269.1:n.844-91G>A
XM_011529968.1:c.844-91G>A	XP_011528270.1:n.844-91G>A
XM_011529969.1:c.700-91G>A	XP_011528271.1:n.700-91G>A
XM_011529970.1:c.691-91G>A	XP_011528272.1:n.691-91G>A
XM_011529971.1:c.700-91G>A	XP_011528273.1:n.700-91G>A
XM_011529972.1:c.843+100G>A	XP_011528274.1:n.843+100G>A
NM_000106.6:c.844-91G>A MANE Select	NP_000097.3:n.844-91G>A
NM_001025161.3:c.691-91G>A	NP_001020332.2:n.691-91G>A