Canonical Allele Identifier: CA411773933

Gene: CYP2D6

Linked Data

• dbSNP Id: rs1931469907
• MyVariant Identifiers: chr22:g.42524862T>A (hg19) ; chr22:g.42128860T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128860T>A , CM000684.2:g.42128860T>A	GRCh38
NC_000022.10:g.42524862T>A , CM000684.1:g.42524862T>A	GRCh37
NC_000022.9:g.40854806T>A	NCBI36
NG_008376.3:g.6132A>T
NG_008376.4:g.6951A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.437A>T	ENSP00000353241.6:p.Tyr146Phe
ENST00000645361.2:c.590A>T MANE Select	ENSP00000496150.1:p.Tyr197Phe
ENST00000359033.4:c.437A>T	ENSP00000351927.4:p.Tyr146Phe
ENST00000360124.9:c.257A>T	ENSP00000353241.5:p.Tyr86Phe
ENST00000360608.9:c.590A>T	ENSP00000353820.5:p.Tyr197Phe
ENST00000389970.7:c.524A>T	ENSP00000374620.4:p.Tyr175Phe
ENST00000488442.1:n.1314A>T
NM_000106.5:c.590A>T	NP_000097.3:p.Tyr197Phe
NM_001025161.2:c.437A>T	NP_001020332.2:p.Tyr146Phe
XM_011529966.1:c.590A>T	XP_011528268.1:p.Tyr197Phe
XM_011529967.1:c.590A>T	XP_011528269.1:p.Tyr197Phe
XM_011529968.1:c.590A>T	XP_011528270.1:p.Tyr197Phe
XM_011529969.1:c.446A>T	XP_011528271.1:p.Tyr149Phe
XM_011529970.1:c.437A>T	XP_011528272.1:p.Tyr146Phe
XM_011529971.1:c.446A>T	XP_011528273.1:p.Tyr149Phe
XM_011529972.1:c.590A>T	XP_011528274.1:p.Tyr197Phe
NM_000106.6:c.590A>T MANE Select	NP_000097.3:p.Tyr197Phe
NM_001025161.3:c.437A>T	NP_001020332.2:p.Tyr146Phe