Canonical Allele Identifier: CA411772980

Gene: CYP2D6

Linked Data

• dbSNP Id: rs749023275
• MyVariant Identifiers: chr22:g.42524176C>G (hg19) ; chr22:g.42128174C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128174C>G , CM000684.2:g.42128174C>G	GRCh38
NC_000022.10:g.42524176C>G , CM000684.1:g.42524176C>G	GRCh37
NC_000022.9:g.40854120C>G	NCBI36
NG_008376.3:g.6818G>C
NG_008376.4:g.7637G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.690G>C	ENSP00000353241.6:p.Lys230Asn
ENST00000645361.2:c.843G>C MANE Select	ENSP00000496150.1:p.Lys281Asn
ENST00000359033.4:c.690G>C	ENSP00000351927.4:p.Lys230Asn
ENST00000360124.9:c.510G>C	ENSP00000353241.5:p.Lys170Asn
ENST00000360608.9:c.843G>C	ENSP00000353820.5:p.Lys281Asn
ENST00000389970.7:c.777G>C	ENSP00000374620.4:p.Lys259Asn
ENST00000488442.1:n.1567G>C
NM_000106.5:c.843G>C	NP_000097.3:p.Lys281Asn
NM_001025161.2:c.690G>C	NP_001020332.2:p.Lys230Asn
XM_011529966.1:c.843G>C	XP_011528268.1:p.Lys281Asn
XM_011529967.1:c.843G>C	XP_011528269.1:p.Lys281Asn
XM_011529968.1:c.843G>C	XP_011528270.1:p.Lys281Asn
XM_011529969.1:c.699G>C	XP_011528271.1:p.Lys233Asn
XM_011529970.1:c.690G>C	XP_011528272.1:p.Lys230Asn
XM_011529971.1:c.699G>C	XP_011528273.1:p.Lys233Asn
XM_011529972.1:c.843G>C	XP_011528274.1:p.Lys281Asn
NM_000106.6:c.843G>C MANE Select	NP_000097.3:p.Lys281Asn
NM_001025161.3:c.690G>C	NP_001020332.2:p.Lys230Asn