Canonical Allele Identifier: CA411774713

Gene: CYP2D6

Linked Data

• dbSNP Id: rs1240215026
• gnomAD v4: 22-42129116-T-A
• MyVariant Identifiers: chr22:g.42525118T>A (hg19) ; chr22:g.42129116T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42129116T>A , CM000684.2:g.42129116T>A	GRCh38
NC_000022.10:g.42525118T>A , CM000684.1:g.42525118T>A	GRCh37
NC_000022.9:g.40855062T>A	NCBI36
NG_008376.3:g.5876A>T
NG_008376.4:g.6695A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.353-172A>T	ENSP00000353241.6:n.353-172A>T
ENST00000645361.2:c.422A>T MANE Select	ENSP00000496150.1:p.Asn141Ile
ENST00000359033.4:c.353-172A>T	ENSP00000351927.4:n.353-172A>T
ENST00000360124.9:c.173-172A>T	ENSP00000353241.5:n.173-172A>T
ENST00000360608.9:c.422A>T	ENSP00000353820.5:p.Asn141Ile
ENST00000389970.7:c.356A>T	ENSP00000374620.4:p.Asn119Ile
ENST00000488442.1:n.1146A>T
NM_000106.5:c.422A>T	NP_000097.3:p.Asn141Ile
NM_001025161.2:c.353-172A>T	NP_001020332.2:n.353-172A>T
XM_011529966.1:c.422A>T	XP_011528268.1:p.Asn141Ile
XM_011529967.1:c.422A>T	XP_011528269.1:p.Asn141Ile
XM_011529968.1:c.422A>T	XP_011528270.1:p.Asn141Ile
XM_011529969.1:c.279A>T	XP_011528271.1:p.Gln93His
XM_011529970.1:c.353-172A>T	XP_011528272.1:n.353-172A>T
XM_011529971.1:c.279A>T	XP_011528273.1:p.Gln93His
XM_011529972.1:c.422A>T	XP_011528274.1:p.Asn141Ile
NM_000106.6:c.422A>T MANE Select	NP_000097.3:p.Asn141Ile
NM_001025161.3:c.353-172A>T	NP_001020332.2:n.353-172A>T