Canonical Allele Identifier: CA753326822

Gene: CYP2D6

Linked Data

• dbSNP Id: rs1202353939
• gnomAD v3: 22-42126560-C-T
• gnomAD v4: 22-42126560-C-T
• MyVariant Identifiers: chr22:g.42126560C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42126560C>T , CM000684.2:g.42126560C>T	GRCh38
NC_000022.10:g.42522562C>T , CM000684.1:g.42522562C>T	GRCh37
NC_000022.9:g.40852506C>T	NCBI36
NG_008376.3:g.8432G>A
NG_008376.4:g.9251G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.1306G>A	ENSP00000353241.6:n.1306G>A
ENST00000645361.2:c.*14G>A MANE Select	ENSP00000496150.1:n.*14G>A
ENST00000359033.4:c.*14G>A	ENSP00000351927.4:n.*14G>A
ENST00000360124.9:c.1126G>A	ENSP00000353241.5:n.1126G>A
ENST00000360608.9:c.*14G>A	ENSP00000353820.5:n.*14G>A
ENST00000389970.7:c.*14G>A	ENSP00000374620.4:n.*14G>A
ENST00000488442.1:n.2232G>A
NM_000106.5:c.*14G>A	NP_000097.3:n.*14G>A
NM_001025161.2:c.*14G>A	NP_001020332.2:n.*14G>A
XM_011529966.1:c.1452+56G>A	XP_011528268.1:n.1452+56G>A
XM_011529967.1:c.1452+56G>A	XP_011528269.1:n.1452+56G>A
XM_011529968.1:c.1452+56G>A	XP_011528270.1:n.1452+56G>A
XM_011529969.1:c.1308+56G>A	XP_011528271.1:n.1308+56G>A
XM_011529970.1:c.1299+56G>A	XP_011528272.1:n.1299+56G>A
XM_011529971.1:c.*14G>A	XP_011528273.1:n.*14G>A
NM_000106.6:c.*14G>A MANE Select	NP_000097.3:n.*14G>A
NM_001025161.3:c.*14G>A	NP_001020332.2:n.*14G>A