Canonical Allele Identifier: CA10265006

Gene: CYP2D6

Linked Data

• dbSNP Id: rs373023674
• ExAC: 22:42524840 C / T
• gnomAD v2: 22-42524840-C-T
• MyVariant Identifiers: chr22:g.42524840C>T (hg19) ; chr22:g.42128838C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128838C>T , CM000684.2:g.42128838C>T	GRCh38
NC_000022.10:g.42524840C>T , CM000684.1:g.42524840C>T	GRCh37
NC_000022.9:g.40854784C>T	NCBI36
NG_008376.3:g.6154G>A
NG_008376.4:g.6973G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.459G>A	ENSP00000353241.6:p.Arg153=
ENST00000645361.2:c.612G>A MANE Select	ENSP00000496150.1:p.Arg204=
ENST00000359033.4:c.459G>A	ENSP00000351927.4:p.Arg153=
ENST00000360124.9:c.279G>A	ENSP00000353241.5:p.Arg93=
ENST00000360608.9:c.612G>A	ENSP00000353820.5:p.Arg204=
ENST00000389970.7:c.546G>A	ENSP00000374620.4:p.Arg182=
ENST00000488442.1:n.1336G>A
NM_000106.5:c.612G>A	NP_000097.3:p.Arg204=
NM_001025161.2:c.459G>A	NP_001020332.2:p.Arg153=
XM_011529966.1:c.612G>A	XP_011528268.1:p.Arg204=
XM_011529967.1:c.612G>A	XP_011528269.1:p.Arg204=
XM_011529968.1:c.612G>A	XP_011528270.1:p.Arg204=
XM_011529969.1:c.468G>A	XP_011528271.1:p.Arg156=
XM_011529970.1:c.459G>A	XP_011528272.1:p.Arg153=
XM_011529971.1:c.468G>A	XP_011528273.1:p.Arg156=
XM_011529972.1:c.612G>A	XP_011528274.1:p.Arg204=
NM_000106.6:c.612G>A MANE Select	NP_000097.3:p.Arg204=
NM_001025161.3:c.459G>A	NP_001020332.2:p.Arg153=