Canonical Allele Identifier: CA411773603

Gene: CYP2D6

Linked Data

• gnomAD v4: 22-42128344-T-C
• MyVariant Identifiers: chr22:g.42524346T>C (hg19) ; chr22:g.42128344T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128344T>C , CM000684.2:g.42128344T>C	GRCh38
NC_000022.10:g.42524346T>C , CM000684.1:g.42524346T>C	GRCh37
NC_000022.9:g.40854290T>C	NCBI36
NG_008376.3:g.6648A>G
NG_008376.4:g.7467A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.520A>G	ENSP00000353241.6:p.Asn174Asp
ENST00000645361.2:c.673A>G MANE Select	ENSP00000496150.1:p.Asn225Asp
ENST00000359033.4:c.520A>G	ENSP00000351927.4:p.Asn174Asp
ENST00000360124.9:c.340A>G	ENSP00000353241.5:p.Asn114Asp
ENST00000360608.9:c.673A>G	ENSP00000353820.5:p.Asn225Asp
ENST00000389970.7:c.607A>G	ENSP00000374620.4:p.Asn203Asp
ENST00000488442.1:n.1397A>G
NM_000106.5:c.673A>G	NP_000097.3:p.Asn225Asp
NM_001025161.2:c.520A>G	NP_001020332.2:p.Asn174Asp
XM_011529966.1:c.673A>G	XP_011528268.1:p.Asn225Asp
XM_011529967.1:c.673A>G	XP_011528269.1:p.Asn225Asp
XM_011529968.1:c.673A>G	XP_011528270.1:p.Asn225Asp
XM_011529969.1:c.529A>G	XP_011528271.1:p.Asn177Asp
XM_011529970.1:c.520A>G	XP_011528272.1:p.Asn174Asp
XM_011529971.1:c.529A>G	XP_011528273.1:p.Asn177Asp
XM_011529972.1:c.673A>G	XP_011528274.1:p.Asn225Asp
NM_000106.6:c.673A>G MANE Select	NP_000097.3:p.Asn225Asp
NM_001025161.3:c.520A>G	NP_001020332.2:p.Asn174Asp