Canonical Allele Identifier: CA10265145
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs766391487

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42129166A>G , CM000684.2:g.42129166A>G GRCh38
NC_000022.10:g.42525168A>G , CM000684.1:g.42525168A>G GRCh37
NC_000022.9:g.40855112A>G NCBI36
NG_008376.3:g.5826T>C
NG_008376.4:g.6645T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000360124.10:c.353-222T>C ENSP00000353241.6:n.353-222T>C
ENST00000645361.2:c.372T>C MANE Select ENSP00000496150.1:p.Tyr124=
ENST00000359033.4:c.353-222T>C ENSP00000351927.4:n.353-222T>C
ENST00000360124.9:c.173-222T>C ENSP00000353241.5:n.173-222T>C
ENST00000360608.9:c.372T>C ENSP00000353820.5:p.Tyr124=
ENST00000389970.7:c.306T>C ENSP00000374620.4:p.Tyr102=
ENST00000488442.1:n.1096T>C
NM_000106.5:c.372T>C NP_000097.3:p.Tyr124=
NM_001025161.2:c.353-222T>C NP_001020332.2:n.353-222T>C
XM_011529966.1:c.372T>C XP_011528268.1:p.Tyr124=
XM_011529967.1:c.372T>C XP_011528269.1:p.Tyr124=
XM_011529968.1:c.372T>C XP_011528270.1:p.Tyr124=
XM_011529969.1:c.229T>C XP_011528271.1:p.Trp77Arg
XM_011529970.1:c.353-222T>C XP_011528272.1:n.353-222T>C
XM_011529971.1:c.229T>C XP_011528273.1:p.Trp77Arg
XM_011529972.1:c.372T>C XP_011528274.1:p.Tyr124=
NM_000106.6:c.372T>C MANE Select NP_000097.3:p.Tyr124=
NM_001025161.3:c.353-222T>C NP_001020332.2:n.353-222T>C