Canonical Allele Identifier: CA2657029084

Gene: CYP2D6

Linked Data

• gnomAD v4: 22-42126515-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42126515G>T , CM000684.2:g.42126515G>T	GRCh38
NC_000022.10:g.42522517G>T , CM000684.1:g.42522517G>T	GRCh37
NC_000022.9:g.40852461G>T	NCBI36
NG_008376.3:g.8477C>A
NG_008376.4:g.9296C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.1351C>A	ENSP00000353241.6:n.1351C>A
ENST00000645361.2:c.*59C>A MANE Select	ENSP00000496150.1:n.*59C>A
ENST00000360124.9:c.1171C>A	ENSP00000353241.5:n.1171C>A
ENST00000360608.9:c.*59C>A	ENSP00000353820.5:n.*59C>A
ENST00000389970.7:c.*59C>A	ENSP00000374620.4:n.*59C>A
NM_000106.5:c.*59C>A	NP_000097.3:n.*59C>A
NM_001025161.2:c.*59C>A	NP_001020332.2:n.*59C>A
XM_011529966.1:c.1452+101C>A	XP_011528268.1:n.1452+101C>A
XM_011529967.1:c.1452+101C>A	XP_011528269.1:n.1452+101C>A
XM_011529968.1:c.1452+101C>A	XP_011528270.1:n.1452+101C>A
XM_011529969.1:c.1308+101C>A	XP_011528271.1:n.1308+101C>A
XM_011529970.1:c.1299+101C>A	XP_011528272.1:n.1299+101C>A
XM_011529971.1:c.*59C>A	XP_011528273.1:n.*59C>A
NM_000106.6:c.*59C>A MANE Select	NP_000097.3:n.*59C>A
NM_001025161.3:c.*59C>A	NP_001020332.2:n.*59C>A