Canonical Allele Identifier: CA10264851

Gene: CYP2D6

Linked Data

• dbSNP Id: rs770790629
• ExAC: 22:42524182 C / T
• MyVariant Identifiers: chr22:g.42524182C>T (hg19) ; chr22:g.42128180C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128180C>T , CM000684.2:g.42128180C>T	GRCh38
NC_000022.10:g.42524182C>T , CM000684.1:g.42524182C>T	GRCh37
NC_000022.9:g.40854126C>T	NCBI36
NG_008376.3:g.6812G>A
NG_008376.4:g.7631G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.684G>A	ENSP00000353241.6:p.Met228Ile
ENST00000645361.2:c.837G>A MANE Select	ENSP00000496150.1:p.Met279Ile
ENST00000359033.4:c.684G>A	ENSP00000351927.4:p.Met228Ile
ENST00000360124.9:c.504G>A	ENSP00000353241.5:p.Met168Ile
ENST00000360608.9:c.837G>A	ENSP00000353820.5:p.Met279Ile
ENST00000389970.7:c.771G>A	ENSP00000374620.4:p.Met257Ile
ENST00000488442.1:n.1561G>A
NM_000106.5:c.837G>A	NP_000097.3:p.Met279Ile
NM_001025161.2:c.684G>A	NP_001020332.2:p.Met228Ile
XM_011529966.1:c.837G>A	XP_011528268.1:p.Met279Ile
XM_011529967.1:c.837G>A	XP_011528269.1:p.Met279Ile
XM_011529968.1:c.837G>A	XP_011528270.1:p.Met279Ile
XM_011529969.1:c.693G>A	XP_011528271.1:p.Met231Ile
XM_011529970.1:c.684G>A	XP_011528272.1:p.Met228Ile
XM_011529971.1:c.693G>A	XP_011528273.1:p.Met231Ile
XM_011529972.1:c.837G>A	XP_011528274.1:p.Met279Ile
NM_000106.6:c.837G>A MANE Select	NP_000097.3:p.Met279Ile
NM_001025161.3:c.684G>A	NP_001020332.2:p.Met228Ile