Canonical Allele Identifier: CA324674773

Gene: CYP2D6

Linked Data

• dbSNP Id: rs28371701
• gnomAD v3: 22-42130047-G-C
• gnomAD v4: 22-42130047-G-C
• MyVariant Identifiers: chr22:g.42130047G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42130047G>C , CM000684.2:g.42130047G>C	GRCh38
NG_008376.3:g.4945C>G
NG_008376.4:g.5764C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.181-138C>G	ENSP00000353241.6:n.181-138C>G
ENST00000645361.2:c.181-138C>G MANE Select	ENSP00000496150.1:n.181-138C>G
ENST00000359033.4:c.181-138C>G	ENSP00000351927.4:n.181-138C>G
ENST00000360608.9:c.181-138C>G	ENSP00000353820.5:n.181-138C>G
ENST00000389970.7:c.115-138C>G	ENSP00000374620.4:n.115-138C>G
ENST00000488442.1:n.767C>G
NM_000106.5:c.181-138C>G	NP_000097.3:n.181-138C>G
NM_001025161.2:c.181-138C>G	NP_001020332.2:n.181-138C>G
XM_011529966.1:c.181-138C>G	XP_011528268.1:n.181-138C>G
XM_011529967.1:c.181-138C>G	XP_011528269.1:n.181-138C>G
XM_011529968.1:c.181-138C>G	XP_011528270.1:n.181-138C>G
XM_011529969.1:c.38-138C>G	XP_011528271.1:n.38-138C>G
XM_011529970.1:c.181-138C>G	XP_011528272.1:n.181-138C>G
XM_011529971.1:c.38-138C>G	XP_011528273.1:n.38-138C>G
XM_011529972.1:c.181-138C>G	XP_011528274.1:n.181-138C>G
XR_430455.2:n.94-64G>C
NM_000106.6:c.181-138C>G MANE Select	NP_000097.3:n.181-138C>G
NM_001025161.3:c.181-138C>G	NP_001020332.2:n.181-138C>G