Canonical Allele Identifier: CA411773774

Gene: CYP2D6

Linked Data

• dbSNP Id: rs201501394
• gnomAD v2: 22-42524802-G-C
• MyVariant Identifiers: chr22:g.42524802G>C (hg19) ; chr22:g.42128800G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128800G>C , CM000684.2:g.42128800G>C	GRCh38
NC_000022.10:g.42524802G>C , CM000684.1:g.42524802G>C	GRCh37
NC_000022.9:g.40854746G>C	NCBI36
NG_008376.3:g.6192C>G
NG_008376.4:g.7011C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.497C>G	ENSP00000353241.6:p.Ser166Trp
ENST00000645361.2:c.650C>G MANE Select	ENSP00000496150.1:p.Ser217Trp
ENST00000359033.4:c.497C>G	ENSP00000351927.4:p.Ser166Trp
ENST00000360124.9:c.317C>G	ENSP00000353241.5:p.Ser106Trp
ENST00000360608.9:c.650C>G	ENSP00000353820.5:p.Ser217Trp
ENST00000389970.7:c.584C>G	ENSP00000374620.4:p.Ser195Trp
ENST00000488442.1:n.1374C>G
NM_000106.5:c.650C>G	NP_000097.3:p.Ser217Trp
NM_001025161.2:c.497C>G	NP_001020332.2:p.Ser166Trp
XM_011529966.1:c.650C>G	XP_011528268.1:p.Ser217Trp
XM_011529967.1:c.650C>G	XP_011528269.1:p.Ser217Trp
XM_011529968.1:c.650C>G	XP_011528270.1:p.Ser217Trp
XM_011529969.1:c.506C>G	XP_011528271.1:p.Ser169Trp
XM_011529970.1:c.497C>G	XP_011528272.1:p.Ser166Trp
XM_011529971.1:c.506C>G	XP_011528273.1:p.Ser169Trp
XM_011529972.1:c.650C>G	XP_011528274.1:p.Ser217Trp
NM_000106.6:c.650C>G MANE Select	NP_000097.3:p.Ser217Trp
NM_001025161.3:c.497C>G	NP_001020332.2:p.Ser166Trp