Canonical Allele Identifier: CA411772492

Gene: CYP2D6

Linked Data

• dbSNP Id: rs2146932792
• MyVariant Identifiers: chr22:g.42523882C>G (hg19) ; chr22:g.42127880C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42127880C>G , CM000684.2:g.42127880C>G	GRCh38
NC_000022.10:g.42523882C>G , CM000684.1:g.42523882C>G	GRCh37
NC_000022.9:g.40853826C>G	NCBI36
NG_008376.3:g.7112G>C
NG_008376.4:g.7931G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.745G>C	ENSP00000353241.6:n.745G>C
ENST00000645361.2:c.947G>C MANE Select	ENSP00000496150.1:p.Trp316Ser
ENST00000359033.4:c.794G>C	ENSP00000351927.4:p.Trp265Ser
ENST00000360124.9:c.565G>C	ENSP00000353241.5:n.565G>C
ENST00000360608.9:c.947G>C	ENSP00000353820.5:p.Trp316Ser
ENST00000389970.7:c.881G>C	ENSP00000374620.4:p.Trp294Ser
ENST00000488442.1:n.1671G>C
NM_000106.5:c.947G>C	NP_000097.3:p.Trp316Ser
NM_001025161.2:c.794G>C	NP_001020332.2:p.Trp265Ser
XM_011529966.1:c.947G>C	XP_011528268.1:p.Trp316Ser
XM_011529967.1:c.947G>C	XP_011528269.1:p.Trp316Ser
XM_011529968.1:c.947G>C	XP_011528270.1:p.Trp316Ser
XM_011529969.1:c.803G>C	XP_011528271.1:p.Trp268Ser
XM_011529970.1:c.794G>C	XP_011528272.1:p.Trp265Ser
XM_011529971.1:c.803G>C	XP_011528273.1:p.Trp268Ser
XM_011529972.1:c.844-246G>C	XP_011528274.1:n.844-246G>C
NM_000106.6:c.947G>C MANE Select	NP_000097.3:p.Trp316Ser
NM_001025161.3:c.794G>C	NP_001020332.2:p.Trp265Ser