Canonical Allele Identifier: CA411773904
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs1379103867
MyVariant Identifiers: chr22:g.42524846G>T (hg19) chr22:g.42128844G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42128844G>T , CM000684.2:g.42128844G>T GRCh38
NC_000022.10:g.42524846G>T , CM000684.1:g.42524846G>T GRCh37
NC_000022.9:g.40854790G>T NCBI36
NG_008376.3:g.6148C>A
NG_008376.4:g.6967C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000360124.10:c.453C>A ENSP00000353241.6:p.Phe151Leu
ENST00000645361.2:c.606C>A MANE Select ENSP00000496150.1:p.Phe202Leu
ENST00000359033.4:c.453C>A ENSP00000351927.4:p.Phe151Leu
ENST00000360124.9:c.273C>A ENSP00000353241.5:p.Phe91Leu
ENST00000360608.9:c.606C>A ENSP00000353820.5:p.Phe202Leu
ENST00000389970.7:c.540C>A ENSP00000374620.4:p.Phe180Leu
ENST00000488442.1:n.1330C>A
NM_000106.5:c.606C>A NP_000097.3:p.Phe202Leu
NM_001025161.2:c.453C>A NP_001020332.2:p.Phe151Leu
XM_011529966.1:c.606C>A XP_011528268.1:p.Phe202Leu
XM_011529967.1:c.606C>A XP_011528269.1:p.Phe202Leu
XM_011529968.1:c.606C>A XP_011528270.1:p.Phe202Leu
XM_011529969.1:c.462C>A XP_011528271.1:p.Phe154Leu
XM_011529970.1:c.453C>A XP_011528272.1:p.Phe151Leu
XM_011529971.1:c.462C>A XP_011528273.1:p.Phe154Leu
XM_011529972.1:c.606C>A XP_011528274.1:p.Phe202Leu
NM_000106.6:c.606C>A MANE Select NP_000097.3:p.Phe202Leu
NM_001025161.3:c.453C>A NP_001020332.2:p.Phe151Leu
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