Canonical Allele Identifier: CA514799847
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs1422318295

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42126616C>T , CM000684.2:g.42126616C>T GRCh38
NC_000022.10:g.42522618C>T , CM000684.1:g.42522618C>T GRCh37
NC_000022.9:g.40852562C>T NCBI36
NG_008376.3:g.8376G>A
NG_008376.4:g.9195G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000360124.10:c.1250G>A ENSP00000353241.6:n.1250G>A
ENST00000645361.2:c.1452G>A MANE Select ENSP00000496150.1:p.Leu484=
ENST00000359033.4:c.1299G>A ENSP00000351927.4:p.Leu433=
ENST00000360124.9:c.1070G>A ENSP00000353241.5:n.1070G>A
ENST00000360608.9:c.1452G>A ENSP00000353820.5:p.Leu484=
ENST00000389970.7:c.1443G>A ENSP00000374620.4:p.Leu481=
ENST00000488442.1:n.2176G>A
NM_000106.5:c.1452G>A NP_000097.3:p.Leu484=
NM_001025161.2:c.1299G>A NP_001020332.2:p.Leu433=
XM_011529966.1:c.1452G>A XP_011528268.1:p.Leu484=
XM_011529967.1:c.1452G>A XP_011528269.1:p.Leu484=
XM_011529968.1:c.1452G>A XP_011528270.1:p.Leu484=
XM_011529969.1:c.1308G>A XP_011528271.1:p.Leu436=
XM_011529970.1:c.1299G>A XP_011528272.1:p.Leu433=
XM_011529971.1:c.1308G>A XP_011528273.1:p.Leu436=
NM_000106.6:c.1452G>A MANE Select NP_000097.3:p.Leu484=
NM_001025161.3:c.1299G>A NP_001020332.2:p.Leu433=