Canonical Allele Identifier: CA324675739

Gene: CYP2D6

Linked Data

• dbSNP Id: rs536049502
• gnomAD v3: 22-42130873-T-A
• gnomAD v4: 22-42130873-T-A
• MyVariant Identifiers: chr22:g.42526875T>A (hg19) ; chr22:g.42130873T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42130873T>A , CM000684.2:g.42130873T>A	GRCh38
NC_000022.10:g.42526875T>A , CM000684.1:g.42526875T>A	GRCh37
NC_000022.9:g.40856819T>A	NCBI36
NG_008376.3:g.4119A>T
NG_008376.4:g.4938A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360608.9:c.-82A>T	ENSP00000353820.5:n.-82A>T
ENST00000389970.7:c.-148A>T	ENSP00000374620.4:n.-148A>T
NM_000106.5:c.-82A>T	NP_000097.3:n.-82A>T
NM_001025161.2:c.-82A>T	NP_001020332.2:n.-82A>T
XM_011529966.1:c.-82A>T	XP_011528268.1:n.-82A>T
XM_011529967.1:c.-82A>T	XP_011528269.1:n.-82A>T
XM_011529968.1:c.-82A>T	XP_011528270.1:n.-82A>T
XM_011529969.1:c.37+424A>T	XP_011528271.1:n.37+424A>T
XM_011529970.1:c.-82A>T	XP_011528272.1:n.-82A>T
XM_011529971.1:c.37+424A>T	XP_011528273.1:n.37+424A>T
XM_011529972.1:c.-82A>T	XP_011528274.1:n.-82A>T
XR_430455.2:n.328+185T>A
XR_002958749.1:n.275+185T>A