Canonical Allele Identifier: CA514799576

Gene: CYP2D6

Linked Data

• gnomAD v4: 22-42126574-C-T
• MyVariant Identifiers: chr22:g.42522576C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42126574C>T , CM000684.2:g.42126574C>T	GRCh38
NC_000022.10:g.42522576C>T , CM000684.1:g.42522576C>T	GRCh37
NC_000022.9:g.40852520C>T	NCBI36
NG_008376.3:g.8418G>A
NG_008376.4:g.9237G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.1292G>A	ENSP00000353241.6:n.1292G>A
ENST00000645361.2:c.1494G>A MANE Select	ENSP00000496150.1:p.Ter498=
ENST00000359033.4:c.1341G>A	ENSP00000351927.4:p.Ter447=
ENST00000360124.9:c.1112G>A	ENSP00000353241.5:n.1112G>A
ENST00000360608.9:c.1494G>A	ENSP00000353820.5:p.Ter498=
ENST00000389970.7:c.1485G>A	ENSP00000374620.4:p.Ter495=
ENST00000488442.1:n.2218G>A
NM_000106.5:c.1494G>A	NP_000097.3:p.Ter498=
NM_001025161.2:c.1341G>A	NP_001020332.2:p.Ter447=
XM_011529966.1:c.1452+42G>A	XP_011528268.1:n.1452+42G>A
XM_011529967.1:c.1452+42G>A	XP_011528269.1:n.1452+42G>A
XM_011529968.1:c.1452+42G>A	XP_011528270.1:n.1452+42G>A
XM_011529969.1:c.1308+42G>A	XP_011528271.1:n.1308+42G>A
XM_011529970.1:c.1299+42G>A	XP_011528272.1:n.1299+42G>A
XM_011529971.1:c.1350G>A	XP_011528273.1:p.Ter450=
NM_000106.6:c.1494G>A MANE Select	NP_000097.3:p.Ter498=
NM_001025161.3:c.1341G>A	NP_001020332.2:p.Ter447=