Canonical Allele Identifier: CA126958
Gene: CYP2D6 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 16894
dbSNP Id: rs35742686

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42128242del , CM000684.2:g.42128242del GRCh38
NC_000022.10:g.42524244del , CM000684.1:g.42524244del GRCh37
NC_000022.9:g.40854188del NCBI36
NG_008376.3:g.6750del
NG_008376.4:g.7569del

Transcript Alleles

HGVS Amino-acid change
NM_000106.5:c.775del VV NP_000097.3:p.Arg259GlyfsTer2
NM_001025161.2:c.622del VV NP_001020332.2:p.Arg208GlyfsTer2
XM_011529966.1:c.775del XP_011528268.1:p.Arg259GlyfsTer2
XM_011529967.1:c.775del XP_011528269.1:p.Arg259GlyfsTer2
XM_011529968.1:c.775del XP_011528270.1:p.Arg259GlyfsTer2
XM_011529969.1:c.631del XP_011528271.1:p.Arg211GlyfsTer2
XM_011529970.1:c.622del XP_011528272.1:p.Arg208GlyfsTer2
XM_011529971.1:c.631del XP_011528273.1:p.Arg211GlyfsTer2
XM_011529972.1:c.775del XP_011528274.1:p.Arg259GlyfsTer2
NM_000106.6:c.775del VV NP_000097.3:p.Arg259GlyfsTer2
ENST00000359033.4:c.622del ENSP00000351927.4:p.Arg208GlyfsTer2
ENST00000360124.9:n.442del ENSP00000353241.5:p.Arg148GlyfsTer2
ENST00000360608.9:c.775del ENSP00000353820.5:p.Arg259GlyfsTer2
ENST00000389970.7:c.709del ENSP00000374620.4:p.Arg237GlyfsTer2
ENST00000488442.1:n.1499del