Canonical Allele Identifier: CA514800282

Gene: CYP2D6

Linked Data

• MyVariant Identifiers: chr22:g.42524218G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128216G>C , CM000684.2:g.42128216G>C	GRCh38
NC_000022.10:g.42524218G>C , CM000684.1:g.42524218G>C	GRCh37
NC_000022.9:g.40854162G>C	NCBI36
NG_008376.3:g.6776C>G
NG_008376.4:g.7595C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.648C>G	ENSP00000353241.6:p.Pro216=
ENST00000645361.2:c.801C>G MANE Select	ENSP00000496150.1:p.Pro267=
ENST00000359033.4:c.648C>G	ENSP00000351927.4:p.Pro216=
ENST00000360124.9:c.468C>G	ENSP00000353241.5:p.Pro156=
ENST00000360608.9:c.801C>G	ENSP00000353820.5:p.Pro267=
ENST00000389970.7:c.735C>G	ENSP00000374620.4:p.Pro245=
ENST00000488442.1:n.1525C>G
NM_000106.5:c.801C>G	NP_000097.3:p.Pro267=
NM_001025161.2:c.648C>G	NP_001020332.2:p.Pro216=
XM_011529966.1:c.801C>G	XP_011528268.1:p.Pro267=
XM_011529967.1:c.801C>G	XP_011528269.1:p.Pro267=
XM_011529968.1:c.801C>G	XP_011528270.1:p.Pro267=
XM_011529969.1:c.657C>G	XP_011528271.1:p.Pro219=
XM_011529970.1:c.648C>G	XP_011528272.1:p.Pro216=
XM_011529971.1:c.657C>G	XP_011528273.1:p.Pro219=
XM_011529972.1:c.801C>G	XP_011528274.1:p.Pro267=
NM_000106.6:c.801C>G MANE Select	NP_000097.3:p.Pro267=
NM_001025161.3:c.648C>G	NP_001020332.2:p.Pro216=