Canonical Allele Identifier: CA10264988
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs770638636

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42128803T>G , CM000684.2:g.42128803T>G GRCh38
NC_000022.10:g.42524805T>G , CM000684.1:g.42524805T>G GRCh37
NC_000022.9:g.40854749T>G NCBI36
NG_008376.3:g.6189A>C
NG_008376.4:g.7008A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000360124.10:c.494A>C ENSP00000353241.6:p.Glu165Ala
ENST00000645361.2:c.647A>C MANE Select ENSP00000496150.1:p.Glu216Ala
ENST00000359033.4:c.494A>C ENSP00000351927.4:p.Glu165Ala
ENST00000360124.9:c.314A>C ENSP00000353241.5:p.Glu105Ala
ENST00000360608.9:c.647A>C ENSP00000353820.5:p.Glu216Ala
ENST00000389970.7:c.581A>C ENSP00000374620.4:p.Glu194Ala
ENST00000488442.1:n.1371A>C
NM_000106.5:c.647A>C NP_000097.3:p.Glu216Ala
NM_001025161.2:c.494A>C NP_001020332.2:p.Glu165Ala
XM_011529966.1:c.647A>C XP_011528268.1:p.Glu216Ala
XM_011529967.1:c.647A>C XP_011528269.1:p.Glu216Ala
XM_011529968.1:c.647A>C XP_011528270.1:p.Glu216Ala
XM_011529969.1:c.503A>C XP_011528271.1:p.Glu168Ala
XM_011529970.1:c.494A>C XP_011528272.1:p.Glu165Ala
XM_011529971.1:c.503A>C XP_011528273.1:p.Glu168Ala
XM_011529972.1:c.647A>C XP_011528274.1:p.Glu216Ala
NM_000106.6:c.647A>C MANE Select NP_000097.3:p.Glu216Ala
NM_001025161.3:c.494A>C NP_001020332.2:p.Glu165Ala