Canonical Allele Identifier: CA411771441

Gene: CYP2D6

Linked Data

• MyVariant Identifiers: chr22:g.42523499T>A (hg19) ; chr22:g.42127497T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42127497T>A , CM000684.2:g.42127497T>A	GRCh38
NC_000022.10:g.42523499T>A , CM000684.1:g.42523499T>A	GRCh37
NC_000022.9:g.40853443T>A	NCBI36
NG_008376.3:g.7495A>T
NG_008376.4:g.8314A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.921A>T	ENSP00000353241.6:n.921A>T
ENST00000645361.2:c.1123A>T MANE Select	ENSP00000496150.1:p.Thr375Ser
ENST00000359033.4:c.970A>T	ENSP00000351927.4:p.Thr324Ser
ENST00000360124.9:c.741A>T	ENSP00000353241.5:n.741A>T
ENST00000360608.9:c.1123A>T	ENSP00000353820.5:p.Thr375Ser
ENST00000389970.7:c.1114A>T	ENSP00000374620.4:p.Thr372Ser
ENST00000488442.1:n.1847A>T
NM_000106.5:c.1123A>T	NP_000097.3:p.Thr375Ser
NM_001025161.2:c.970A>T	NP_001020332.2:p.Thr324Ser
XM_011529966.1:c.1123A>T	XP_011528268.1:p.Thr375Ser
XM_011529967.1:c.1123A>T	XP_011528269.1:p.Thr375Ser
XM_011529968.1:c.1123A>T	XP_011528270.1:p.Thr375Ser
XM_011529969.1:c.979A>T	XP_011528271.1:p.Thr327Ser
XM_011529970.1:c.970A>T	XP_011528272.1:p.Thr324Ser
XM_011529971.1:c.979A>T	XP_011528273.1:p.Thr327Ser
NM_000106.6:c.1123A>T MANE Select	NP_000097.3:p.Thr375Ser
NM_001025161.3:c.970A>T	NP_001020332.2:p.Thr324Ser