Canonical Allele Identifier: CA411773765

Gene: CYP2D6

Linked Data

• dbSNP Id: rs1291448337
• gnomAD v2: 22-42524799-C-A
• MyVariant Identifiers: chr22:g.42524799C>A (hg19) ; chr22:g.42128797C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128797C>A , CM000684.2:g.42128797C>A	GRCh38
NC_000022.10:g.42524799C>A , CM000684.1:g.42524799C>A	GRCh37
NC_000022.9:g.40854743C>A	NCBI36
NG_008376.3:g.6195G>T
NG_008376.4:g.7014G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.500G>T	ENSP00000353241.6:p.Gly167Val
ENST00000645361.2:c.653G>T MANE Select	ENSP00000496150.1:p.Gly218Val
ENST00000359033.4:c.500G>T	ENSP00000351927.4:p.Gly167Val
ENST00000360124.9:c.320G>T	ENSP00000353241.5:p.Gly107Val
ENST00000360608.9:c.653G>T	ENSP00000353820.5:p.Gly218Val
ENST00000389970.7:c.587G>T	ENSP00000374620.4:p.Gly196Val
ENST00000488442.1:n.1377G>T
NM_000106.5:c.653G>T	NP_000097.3:p.Gly218Val
NM_001025161.2:c.500G>T	NP_001020332.2:p.Gly167Val
XM_011529966.1:c.653G>T	XP_011528268.1:p.Gly218Val
XM_011529967.1:c.653G>T	XP_011528269.1:p.Gly218Val
XM_011529968.1:c.653G>T	XP_011528270.1:p.Gly218Val
XM_011529969.1:c.509G>T	XP_011528271.1:p.Gly170Val
XM_011529970.1:c.500G>T	XP_011528272.1:p.Gly167Val
XM_011529971.1:c.509G>T	XP_011528273.1:p.Gly170Val
XM_011529972.1:c.653G>T	XP_011528274.1:p.Gly218Val
NM_000106.6:c.653G>T MANE Select	NP_000097.3:p.Gly218Val
NM_001025161.3:c.500G>T	NP_001020332.2:p.Gly167Val