Canonical Allele Identifier: CA411774011

Gene: CYP2D6

Linked Data

• dbSNP Id: rs767893111
• gnomAD v2: 22-42524902-T-G
• gnomAD v4: 22-42128900-T-G
• MyVariant Identifiers: chr22:g.42524902T>G (hg19) ; chr22:g.42128900T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128900T>G , CM000684.2:g.42128900T>G	GRCh38
NC_000022.10:g.42524902T>G , CM000684.1:g.42524902T>G	GRCh37
NC_000022.9:g.40854846T>G	NCBI36
NG_008376.3:g.6092A>C
NG_008376.4:g.6911A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.397A>C	ENSP00000353241.6:p.Asn133His
ENST00000645361.2:c.550A>C MANE Select	ENSP00000496150.1:p.Asn184His
ENST00000359033.4:c.397A>C	ENSP00000351927.4:p.Asn133His
ENST00000360124.9:c.217A>C	ENSP00000353241.5:p.Asn73His
ENST00000360608.9:c.550A>C	ENSP00000353820.5:p.Asn184His
ENST00000389970.7:c.484A>C	ENSP00000374620.4:p.Asn162His
ENST00000488442.1:n.1274A>C
NM_000106.5:c.550A>C	NP_000097.3:p.Asn184His
NM_001025161.2:c.397A>C	NP_001020332.2:p.Asn133His
XM_011529966.1:c.550A>C	XP_011528268.1:p.Asn184His
XM_011529967.1:c.550A>C	XP_011528269.1:p.Asn184His
XM_011529968.1:c.550A>C	XP_011528270.1:p.Asn184His
XM_011529969.1:c.406A>C	XP_011528271.1:p.Asn136His
XM_011529970.1:c.397A>C	XP_011528272.1:p.Asn133His
XM_011529971.1:c.406A>C	XP_011528273.1:p.Asn136His
XM_011529972.1:c.550A>C	XP_011528274.1:p.Asn184His
NM_000106.6:c.550A>C MANE Select	NP_000097.3:p.Asn184His
NM_001025161.3:c.397A>C	NP_001020332.2:p.Asn133His