Canonical Allele Identifier: CA411769817

Gene: CYP2D6

Linked Data

• dbSNP Id: rs1135840
• MyVariant Identifiers: chr22:g.42126611C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42126611C>A , CM000684.2:g.42126611C>A	GRCh38
NG_008376.3:g.8381G>T
NG_008376.4:g.9200G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.1255G>T	ENSP00000353241.6:n.1255G>T
ENST00000645361.2:c.1457G>T MANE Select	ENSP00000496150.1:p.Ser486Ile
ENST00000359033.4:c.1304G>T	ENSP00000351927.4:p.Ser435Ile
ENST00000360124.9:c.1075G>T	ENSP00000353241.5:n.1075G>T
ENST00000360608.9:c.1457G>T	ENSP00000353820.5:p.Ser486Ile
ENST00000389970.7:c.1448G>T	ENSP00000374620.4:p.Ser483Ile
ENST00000488442.1:n.2181G>T
NM_000106.5:c.1457G>T	NP_000097.3:p.Ser486Ile
NM_001025161.2:c.1304G>T	NP_001020332.2:p.Ser435Ile
XM_011529966.1:c.1452+5G>T	XP_011528268.1:n.1452+5G>T
XM_011529967.1:c.1452+5G>T	XP_011528269.1:n.1452+5G>T
XM_011529968.1:c.1452+5G>T	XP_011528270.1:n.1452+5G>T
XM_011529969.1:c.1308+5G>T	XP_011528271.1:n.1308+5G>T
XM_011529970.1:c.1299+5G>T	XP_011528272.1:n.1299+5G>T
XM_011529971.1:c.1313G>T	XP_011528273.1:p.Ser438Ile
NM_000106.6:c.1457G>T MANE Select	NP_000097.3:p.Ser486Ile
NM_001025161.3:c.1304G>T	NP_001020332.2:p.Ser435Ile