Canonical Allele Identifier: CA411773936
Gene: CYP2D6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42128861A>C , CM000684.2:g.42128861A>C GRCh38
NC_000022.10:g.42524863A>C , CM000684.1:g.42524863A>C GRCh37
NC_000022.9:g.40854807A>C NCBI36
NG_008376.3:g.6131T>G
NG_008376.4:g.6950T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000360124.10:c.436T>G ENSP00000353241.6:p.Tyr146Asp
ENST00000645361.2:c.589T>G MANE Select ENSP00000496150.1:p.Tyr197Asp
ENST00000359033.4:c.436T>G ENSP00000351927.4:p.Tyr146Asp
ENST00000360124.9:c.256T>G ENSP00000353241.5:p.Tyr86Asp
ENST00000360608.9:c.589T>G ENSP00000353820.5:p.Tyr197Asp
ENST00000389970.7:c.523T>G ENSP00000374620.4:p.Tyr175Asp
ENST00000488442.1:n.1313T>G
NM_000106.5:c.589T>G NP_000097.3:p.Tyr197Asp
NM_001025161.2:c.436T>G NP_001020332.2:p.Tyr146Asp
XM_011529966.1:c.589T>G XP_011528268.1:p.Tyr197Asp
XM_011529967.1:c.589T>G XP_011528269.1:p.Tyr197Asp
XM_011529968.1:c.589T>G XP_011528270.1:p.Tyr197Asp
XM_011529969.1:c.445T>G XP_011528271.1:p.Tyr149Asp
XM_011529970.1:c.436T>G XP_011528272.1:p.Tyr146Asp
XM_011529971.1:c.445T>G XP_011528273.1:p.Tyr149Asp
XM_011529972.1:c.589T>G XP_011528274.1:p.Tyr197Asp
NM_000106.6:c.589T>G MANE Select NP_000097.3:p.Tyr197Asp
NM_001025161.3:c.436T>G NP_001020332.2:p.Tyr146Asp