Canonical Allele Identifier: CA753331379

Gene: CYP2D6

Linked Data

• dbSNP Id: rs1450718033
• gnomAD v3: 22-42130456-C-A
• gnomAD v4: 22-42130456-C-A
• MyVariant Identifiers: chr22:g.42130456C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42130456C>A , CM000684.2:g.42130456C>A	GRCh38
NC_000022.10:g.42526458C>A , CM000684.1:g.42526458C>A	GRCh37
NC_000022.9:g.40856402C>A	NCBI36
NG_008376.3:g.4536G>T
NG_008376.4:g.5355G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.180+156G>T	ENSP00000353241.6:n.180+156G>T
ENST00000645361.2:c.180+156G>T MANE Select	ENSP00000496150.1:n.180+156G>T
ENST00000359033.4:c.180+156G>T	ENSP00000351927.4:n.180+156G>T
ENST00000360608.9:c.180+156G>T	ENSP00000353820.5:n.180+156G>T
ENST00000389970.7:c.114+156G>T	ENSP00000374620.4:n.114+156G>T
ENST00000488442.1:n.358G>T
NM_000106.5:c.180+156G>T	NP_000097.3:n.180+156G>T
NM_001025161.2:c.180+156G>T	NP_001020332.2:n.180+156G>T
XM_011529966.1:c.180+156G>T	XP_011528268.1:n.180+156G>T
XM_011529967.1:c.180+156G>T	XP_011528269.1:n.180+156G>T
XM_011529968.1:c.180+156G>T	XP_011528270.1:n.180+156G>T
XM_011529969.1:c.38-547G>T	XP_011528271.1:n.38-547G>T
XM_011529970.1:c.180+156G>T	XP_011528272.1:n.180+156G>T
XM_011529971.1:c.38-547G>T	XP_011528273.1:n.38-547G>T
XM_011529972.1:c.180+156G>T	XP_011528274.1:n.180+156G>T
XR_430455.2:n.207-111C>A
NM_000106.6:c.180+156G>T MANE Select	NP_000097.3:n.180+156G>T
XR_002958749.1:n.154-111C>A
NM_001025161.3:c.180+156G>T	NP_001020332.2:n.180+156G>T