Canonical Allele Identifier: CA514800259

Gene: CYP2D6

Linked Data

• MyVariant Identifiers: chr22:g.42523983G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42127981G>C , CM000684.2:g.42127981G>C	GRCh38
NC_000022.10:g.42523983G>C , CM000684.1:g.42523983G>C	GRCh37
NC_000022.9:g.40853927G>C	NCBI36
NG_008376.3:g.7011C>G
NG_008376.4:g.7830C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.691-47C>G	ENSP00000353241.6:n.691-47C>G
ENST00000645361.2:c.846C>G MANE Select	ENSP00000496150.1:p.Ala282=
ENST00000359033.4:c.693C>G	ENSP00000351927.4:p.Ala231=
ENST00000360124.9:c.511-47C>G	ENSP00000353241.5:n.511-47C>G
ENST00000360608.9:c.846C>G	ENSP00000353820.5:p.Ala282=
ENST00000389970.7:c.780C>G	ENSP00000374620.4:p.Ala260=
ENST00000488442.1:n.1570C>G
NM_000106.5:c.846C>G	NP_000097.3:p.Ala282=
NM_001025161.2:c.693C>G	NP_001020332.2:p.Ala231=
XM_011529966.1:c.846C>G	XP_011528268.1:p.Ala282=
XM_011529967.1:c.846C>G	XP_011528269.1:p.Ala282=
XM_011529968.1:c.846C>G	XP_011528270.1:p.Ala282=
XM_011529969.1:c.702C>G	XP_011528271.1:p.Ala234=
XM_011529970.1:c.693C>G	XP_011528272.1:p.Ala231=
XM_011529971.1:c.702C>G	XP_011528273.1:p.Ala234=
XM_011529972.1:c.843+193C>G	XP_011528274.1:n.843+193C>G
NM_000106.6:c.846C>G MANE Select	NP_000097.3:p.Ala282=
NM_001025161.3:c.693C>G	NP_001020332.2:p.Ala231=