Canonical Allele Identifier: CA514800385

Gene: CYP2D6

Linked Data

• MyVariant Identifiers: chr22:g.42523875G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42127873G>C , CM000684.2:g.42127873G>C	GRCh38
NC_000022.10:g.42523875G>C , CM000684.1:g.42523875G>C	GRCh37
NC_000022.9:g.40853819G>C	NCBI36
NG_008376.3:g.7119C>G
NG_008376.4:g.7938C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.752C>G	ENSP00000353241.6:n.752C>G
ENST00000645361.2:c.954C>G MANE Select	ENSP00000496150.1:p.Leu318=
ENST00000359033.4:c.801C>G	ENSP00000351927.4:p.Leu267=
ENST00000360124.9:c.572C>G	ENSP00000353241.5:n.572C>G
ENST00000360608.9:c.954C>G	ENSP00000353820.5:p.Leu318=
ENST00000389970.7:c.888C>G	ENSP00000374620.4:p.Leu296=
ENST00000488442.1:n.1678C>G
NM_000106.5:c.954C>G	NP_000097.3:p.Leu318=
NM_001025161.2:c.801C>G	NP_001020332.2:p.Leu267=
XM_011529966.1:c.954C>G	XP_011528268.1:p.Leu318=
XM_011529967.1:c.954C>G	XP_011528269.1:p.Leu318=
XM_011529968.1:c.954C>G	XP_011528270.1:p.Leu318=
XM_011529969.1:c.810C>G	XP_011528271.1:p.Leu270=
XM_011529970.1:c.801C>G	XP_011528272.1:p.Leu267=
XM_011529971.1:c.810C>G	XP_011528273.1:p.Leu270=
XM_011529972.1:c.844-239C>G	XP_011528274.1:n.844-239C>G
NM_000106.6:c.954C>G MANE Select	NP_000097.3:p.Leu318=
NM_001025161.3:c.801C>G	NP_001020332.2:p.Leu267=