Canonical Allele Identifier: CA411773178
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs1323341780

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42128218G>A , CM000684.2:g.42128218G>A GRCh38
NC_000022.10:g.42524220G>A , CM000684.1:g.42524220G>A GRCh37
NC_000022.9:g.40854164G>A NCBI36
NG_008376.3:g.6774C>T
NG_008376.4:g.7593C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000360124.10:c.646C>T ENSP00000353241.6:p.Pro216Ser
ENST00000645361.2:c.799C>T MANE Select ENSP00000496150.1:p.Pro267Ser
ENST00000359033.4:c.646C>T ENSP00000351927.4:p.Pro216Ser
ENST00000360124.9:c.466C>T ENSP00000353241.5:p.Pro156Ser
ENST00000360608.9:c.799C>T ENSP00000353820.5:p.Pro267Ser
ENST00000389970.7:c.733C>T ENSP00000374620.4:p.Pro245Ser
ENST00000488442.1:n.1523C>T
NM_000106.5:c.799C>T NP_000097.3:p.Pro267Ser
NM_001025161.2:c.646C>T NP_001020332.2:p.Pro216Ser
XM_011529966.1:c.799C>T XP_011528268.1:p.Pro267Ser
XM_011529967.1:c.799C>T XP_011528269.1:p.Pro267Ser
XM_011529968.1:c.799C>T XP_011528270.1:p.Pro267Ser
XM_011529969.1:c.655C>T XP_011528271.1:p.Pro219Ser
XM_011529970.1:c.646C>T XP_011528272.1:p.Pro216Ser
XM_011529971.1:c.655C>T XP_011528273.1:p.Pro219Ser
XM_011529972.1:c.799C>T XP_011528274.1:p.Pro267Ser
NM_000106.6:c.799C>T MANE Select NP_000097.3:p.Pro267Ser
NM_001025161.3:c.646C>T NP_001020332.2:p.Pro216Ser