Canonical Allele Identifier: CA411773189

Gene: CYP2D6

Linked Data

• dbSNP Id: rs1931283455
• gnomAD v3: 22-42128221-G-A
• gnomAD v4: 22-42128221-G-A
• MyVariant Identifiers: chr22:g.42524223G>A (hg19) ; chr22:g.42128221G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128221G>A , CM000684.2:g.42128221G>A	GRCh38
NC_000022.10:g.42524223G>A , CM000684.1:g.42524223G>A	GRCh37
NC_000022.9:g.40854167G>A	NCBI36
NG_008376.3:g.6771C>T
NG_008376.4:g.7590C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.643C>T	ENSP00000353241.6:p.Gln215Ter
ENST00000645361.2:c.796C>T MANE Select	ENSP00000496150.1:p.Gln266Ter
ENST00000359033.4:c.643C>T	ENSP00000351927.4:p.Gln215Ter
ENST00000360124.9:c.463C>T	ENSP00000353241.5:p.Gln155Ter
ENST00000360608.9:c.796C>T	ENSP00000353820.5:p.Gln266Ter
ENST00000389970.7:c.730C>T	ENSP00000374620.4:p.Gln244Ter
ENST00000488442.1:n.1520C>T
NM_000106.5:c.796C>T	NP_000097.3:p.Gln266Ter
NM_001025161.2:c.643C>T	NP_001020332.2:p.Gln215Ter
XM_011529966.1:c.796C>T	XP_011528268.1:p.Gln266Ter
XM_011529967.1:c.796C>T	XP_011528269.1:p.Gln266Ter
XM_011529968.1:c.796C>T	XP_011528270.1:p.Gln266Ter
XM_011529969.1:c.652C>T	XP_011528271.1:p.Gln218Ter
XM_011529970.1:c.643C>T	XP_011528272.1:p.Gln215Ter
XM_011529971.1:c.652C>T	XP_011528273.1:p.Gln218Ter
XM_011529972.1:c.796C>T	XP_011528274.1:p.Gln266Ter
NM_000106.6:c.796C>T MANE Select	NP_000097.3:p.Gln266Ter
NM_001025161.3:c.643C>T	NP_001020332.2:p.Gln215Ter