Canonical Allele Identifier: CA411774767

Gene: CYP2D6

Linked Data

• dbSNP Id: rs1931563375
• gnomAD v4: 22-42129142-C-A
• MyVariant Identifiers: chr22:g.42525144C>A (hg19) ; chr22:g.42129142C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42129142C>A , CM000684.2:g.42129142C>A	GRCh38
NC_000022.10:g.42525144C>A , CM000684.1:g.42525144C>A	GRCh37
NC_000022.9:g.40855088C>A	NCBI36
NG_008376.3:g.5850G>T
NG_008376.4:g.6669G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.353-198G>T	ENSP00000353241.6:n.353-198G>T
ENST00000645361.2:c.396G>T MANE Select	ENSP00000496150.1:p.Arg132Ser
ENST00000359033.4:c.353-198G>T	ENSP00000351927.4:n.353-198G>T
ENST00000360124.9:c.173-198G>T	ENSP00000353241.5:n.173-198G>T
ENST00000360608.9:c.396G>T	ENSP00000353820.5:p.Arg132Ser
ENST00000389970.7:c.330G>T	ENSP00000374620.4:p.Arg110Ser
ENST00000488442.1:n.1120G>T
NM_000106.5:c.396G>T	NP_000097.3:p.Arg132Ser
NM_001025161.2:c.353-198G>T	NP_001020332.2:n.353-198G>T
XM_011529966.1:c.396G>T	XP_011528268.1:p.Arg132Ser
XM_011529967.1:c.396G>T	XP_011528269.1:p.Arg132Ser
XM_011529968.1:c.396G>T	XP_011528270.1:p.Arg132Ser
XM_011529969.1:c.253G>T	XP_011528271.1:p.Ala85Ser
XM_011529970.1:c.353-198G>T	XP_011528272.1:n.353-198G>T
XM_011529971.1:c.253G>T	XP_011528273.1:p.Ala85Ser
XM_011529972.1:c.396G>T	XP_011528274.1:p.Arg132Ser
NM_000106.6:c.396G>T MANE Select	NP_000097.3:p.Arg132Ser
NM_001025161.3:c.353-198G>T	NP_001020332.2:n.353-198G>T