Canonical Allele Identifier: CA411772345
Gene: CYP2D6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42127845G>C , CM000684.2:g.42127845G>C GRCh38
NC_000022.10:g.42523847G>C , CM000684.1:g.42523847G>C GRCh37
NC_000022.9:g.40853791G>C NCBI36
NG_008376.3:g.7147C>G
NG_008376.4:g.7966C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000360124.10:c.780C>G ENSP00000353241.6:n.780C>G
ENST00000645361.2:c.982C>G MANE Select ENSP00000496150.1:p.Gln328Glu
ENST00000359033.4:c.829C>G ENSP00000351927.4:p.Gln277Glu
ENST00000360124.9:c.600C>G ENSP00000353241.5:n.600C>G
ENST00000360608.9:c.982C>G ENSP00000353820.5:p.Gln328Glu
ENST00000389970.7:c.916C>G ENSP00000374620.4:p.Gln306Glu
ENST00000488442.1:n.1706C>G
NM_000106.5:c.982C>G NP_000097.3:p.Gln328Glu
NM_001025161.2:c.829C>G NP_001020332.2:p.Gln277Glu
XM_011529966.1:c.982C>G XP_011528268.1:p.Gln328Glu
XM_011529967.1:c.982C>G XP_011528269.1:p.Gln328Glu
XM_011529968.1:c.982C>G XP_011528270.1:p.Gln328Glu
XM_011529969.1:c.838C>G XP_011528271.1:p.Gln280Glu
XM_011529970.1:c.829C>G XP_011528272.1:p.Gln277Glu
XM_011529971.1:c.838C>G XP_011528273.1:p.Gln280Glu
XM_011529972.1:c.844-211C>G XP_011528274.1:n.844-211C>G
NM_000106.6:c.982C>G MANE Select NP_000097.3:p.Gln328Glu
NM_001025161.3:c.829C>G NP_001020332.2:p.Gln277Glu