Canonical Allele Identifier: CA2577737068

Gene: CYP2D6

Linked Data

• gnomAD v4: 22-42126516-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42126516C>T , CM000684.2:g.42126516C>T	GRCh38
NC_000022.10:g.42522518C>T , CM000684.1:g.42522518C>T	GRCh37
NC_000022.9:g.40852462C>T	NCBI36
NG_008376.3:g.8476G>A
NG_008376.4:g.9295G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.1350G>A	ENSP00000353241.6:n.1350G>A
ENST00000645361.2:c.*58G>A MANE Select	ENSP00000496150.1:n.*58G>A
ENST00000360124.9:c.1170G>A	ENSP00000353241.5:n.1170G>A
ENST00000360608.9:c.*58G>A	ENSP00000353820.5:n.*58G>A
ENST00000389970.7:c.*58G>A	ENSP00000374620.4:n.*58G>A
NM_000106.5:c.*58G>A	NP_000097.3:n.*58G>A
NM_001025161.2:c.*58G>A	NP_001020332.2:n.*58G>A
XM_011529966.1:c.1452+100G>A	XP_011528268.1:n.1452+100G>A
XM_011529967.1:c.1452+100G>A	XP_011528269.1:n.1452+100G>A
XM_011529968.1:c.1452+100G>A	XP_011528270.1:n.1452+100G>A
XM_011529969.1:c.1308+100G>A	XP_011528271.1:n.1308+100G>A
XM_011529970.1:c.1299+100G>A	XP_011528272.1:n.1299+100G>A
XM_011529971.1:c.*58G>A	XP_011528273.1:n.*58G>A
NM_000106.6:c.*58G>A MANE Select	NP_000097.3:n.*58G>A
NM_001025161.3:c.*58G>A	NP_001020332.2:n.*58G>A