Canonical Allele Identifier: CA514696604

Gene: CYP2D6

Linked Data

• dbSNP Id: rs757507668
• MyVariant Identifiers: chr22:g.42524789G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128787G>C , CM000684.2:g.42128787G>C	GRCh38
NC_000022.10:g.42524789G>C , CM000684.1:g.42524789G>C	GRCh37
NC_000022.9:g.40854733G>C	NCBI36
NG_008376.3:g.6205C>G
NG_008376.4:g.7024C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.510C>G	ENSP00000353241.6:p.Arg170=
ENST00000645361.2:c.663C>G MANE Select	ENSP00000496150.1:p.Arg221=
ENST00000359033.4:c.510C>G	ENSP00000351927.4:p.Arg170=
ENST00000360124.9:c.330C>G	ENSP00000353241.5:p.Arg110=
ENST00000360608.9:c.663C>G	ENSP00000353820.5:p.Arg221=
ENST00000389970.7:c.597C>G	ENSP00000374620.4:p.Arg199=
ENST00000488442.1:n.1387C>G
NM_000106.5:c.663C>G	NP_000097.3:p.Arg221=
NM_001025161.2:c.510C>G	NP_001020332.2:p.Arg170=
XM_011529966.1:c.663C>G	XP_011528268.1:p.Arg221=
XM_011529967.1:c.663C>G	XP_011528269.1:p.Arg221=
XM_011529968.1:c.663C>G	XP_011528270.1:p.Arg221=
XM_011529969.1:c.519C>G	XP_011528271.1:p.Arg173=
XM_011529970.1:c.510C>G	XP_011528272.1:p.Arg170=
XM_011529971.1:c.519C>G	XP_011528273.1:p.Arg173=
XM_011529972.1:c.663C>G	XP_011528274.1:p.Arg221=
NM_000106.6:c.663C>G MANE Select	NP_000097.3:p.Arg221=
NM_001025161.3:c.510C>G	NP_001020332.2:p.Arg170=