Canonical Allele Identifier: CA753332182

Gene: CYP2D6

Linked Data

• dbSNP Id: rs1164880307
• gnomAD v3: 22-42131083-G-GT
• gnomAD v4: 22-42131083-G-GT
• MyVariant Identifiers: chr22:g.42131083_42131084insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42131084dup , CM000684.2:g.42131084dup	GRCh38
NC_000022.10:g.42527086dup , CM000684.1:g.42527086dup	GRCh37
NC_000022.9:g.40857030dup	NCBI36
NG_008376.3:g.3908dup
NG_008376.4:g.4727dup

Transcript Alleles

HGVS	Amino-acid Change
XM_011529966.1:c.-293dup	XP_011528268.1:n.-293dup
XM_011529967.1:c.-293dup	XP_011528269.1:n.-293dup
XM_011529968.1:c.-293dup	XP_011528270.1:n.-293dup
XM_011529969.1:c.37+213dup	XP_011528271.1:n.37+213dup
XM_011529970.1:c.-293dup	XP_011528272.1:n.-293dup
XM_011529971.1:c.37+213dup	XP_011528273.1:n.37+213dup
XM_011529972.1:c.-293dup	XP_011528274.1:n.-293dup
XR_430455.2:n.328+396dup
XR_002958749.1:n.275+396dup