Canonical Allele Identifier: CA411773113

Gene: CYP2D6

Linked Data

• MyVariant Identifiers: chr22:g.42524204G>T (hg19) ; chr22:g.42128202G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128202G>T , CM000684.2:g.42128202G>T	GRCh38
NC_000022.10:g.42524204G>T , CM000684.1:g.42524204G>T	GRCh37
NC_000022.9:g.40854148G>T	NCBI36
NG_008376.3:g.6790C>A
NG_008376.4:g.7609C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.662C>A	ENSP00000353241.6:p.Thr221Asn
ENST00000645361.2:c.815C>A MANE Select	ENSP00000496150.1:p.Thr272Asn
ENST00000359033.4:c.662C>A	ENSP00000351927.4:p.Thr221Asn
ENST00000360124.9:c.482C>A	ENSP00000353241.5:p.Thr161Asn
ENST00000360608.9:c.815C>A	ENSP00000353820.5:p.Thr272Asn
ENST00000389970.7:c.749C>A	ENSP00000374620.4:p.Thr250Asn
ENST00000488442.1:n.1539C>A
NM_000106.5:c.815C>A	NP_000097.3:p.Thr272Asn
NM_001025161.2:c.662C>A	NP_001020332.2:p.Thr221Asn
XM_011529966.1:c.815C>A	XP_011528268.1:p.Thr272Asn
XM_011529967.1:c.815C>A	XP_011528269.1:p.Thr272Asn
XM_011529968.1:c.815C>A	XP_011528270.1:p.Thr272Asn
XM_011529969.1:c.671C>A	XP_011528271.1:p.Thr224Asn
XM_011529970.1:c.662C>A	XP_011528272.1:p.Thr221Asn
XM_011529971.1:c.671C>A	XP_011528273.1:p.Thr224Asn
XM_011529972.1:c.815C>A	XP_011528274.1:p.Thr272Asn
NM_000106.6:c.815C>A MANE Select	NP_000097.3:p.Thr272Asn
NM_001025161.3:c.662C>A	NP_001020332.2:p.Thr221Asn