Canonical Allele Identifier: CA411769753
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs1440526469

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42126578C>G , CM000684.2:g.42126578C>G GRCh38
NC_000022.10:g.42522580C>G , CM000684.1:g.42522580C>G GRCh37
NC_000022.9:g.40852524C>G NCBI36
NG_008376.3:g.8414G>C
NG_008376.4:g.9233G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000360124.10:c.1288G>C ENSP00000353241.6:n.1288G>C
ENST00000645361.2:c.1490G>C MANE Select ENSP00000496150.1:p.Arg497Pro
ENST00000359033.4:c.1337G>C ENSP00000351927.4:p.Arg446Pro
ENST00000360124.9:c.1108G>C ENSP00000353241.5:n.1108G>C
ENST00000360608.9:c.1490G>C ENSP00000353820.5:p.Arg497Pro
ENST00000389970.7:c.1481G>C ENSP00000374620.4:p.Arg494Pro
ENST00000488442.1:n.2214G>C
NM_000106.5:c.1490G>C NP_000097.3:p.Arg497Pro
NM_001025161.2:c.1337G>C NP_001020332.2:p.Arg446Pro
XM_011529966.1:c.1452+38G>C XP_011528268.1:n.1452+38G>C
XM_011529967.1:c.1452+38G>C XP_011528269.1:n.1452+38G>C
XM_011529968.1:c.1452+38G>C XP_011528270.1:n.1452+38G>C
XM_011529969.1:c.1308+38G>C XP_011528271.1:n.1308+38G>C
XM_011529970.1:c.1299+38G>C XP_011528272.1:n.1299+38G>C
XM_011529971.1:c.1346G>C XP_011528273.1:p.Arg449Pro
NM_000106.6:c.1490G>C MANE Select NP_000097.3:p.Arg497Pro
NM_001025161.3:c.1337G>C NP_001020332.2:p.Arg446Pro