Canonical Allele Identifier: CA324672765

Gene: CYP2D6

Linked Data

• dbSNP Id: rs933264010
• gnomAD v3: 22-42129094-C-T
• gnomAD v4: 22-42129094-C-T
• COSMIC: COSM4675950
• MyVariant Identifiers: chr22:g.42525096C>T (hg19) ; chr22:g.42129094C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42129094C>T , CM000684.2:g.42129094C>T	GRCh38
NC_000022.10:g.42525096C>T , CM000684.1:g.42525096C>T	GRCh37
NC_000022.9:g.40855040C>T	NCBI36
NG_008376.3:g.5898G>A
NG_008376.4:g.6717G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.353-150G>A	ENSP00000353241.6:n.353-150G>A
ENST00000645361.2:c.444G>A MANE Select	ENSP00000496150.1:p.Ser148=
ENST00000359033.4:c.353-150G>A	ENSP00000351927.4:n.353-150G>A
ENST00000360124.9:c.173-150G>A	ENSP00000353241.5:n.173-150G>A
ENST00000360608.9:c.444G>A	ENSP00000353820.5:p.Ser148=
ENST00000389970.7:c.378G>A	ENSP00000374620.4:p.Ser126=
ENST00000488442.1:n.1168G>A
NM_000106.5:c.444G>A	NP_000097.3:p.Ser148=
NM_001025161.2:c.353-150G>A	NP_001020332.2:n.353-150G>A
XM_011529966.1:c.444G>A	XP_011528268.1:p.Ser148=
XM_011529967.1:c.444G>A	XP_011528269.1:p.Ser148=
XM_011529968.1:c.444G>A	XP_011528270.1:p.Ser148=
XM_011529969.1:c.301G>A	XP_011528271.1:p.Ala101Thr
XM_011529970.1:c.353-150G>A	XP_011528272.1:n.353-150G>A
XM_011529971.1:c.301G>A	XP_011528273.1:p.Ala101Thr
XM_011529972.1:c.444G>A	XP_011528274.1:p.Ser148=
NM_000106.6:c.444G>A MANE Select	NP_000097.3:p.Ser148=
NM_001025161.3:c.353-150G>A	NP_001020332.2:n.353-150G>A