Canonical Allele Identifier: CA639828047

Gene: CYP2D6

Linked Data

• dbSNP Id: rs1293358439
• gnomAD v2: 22-42523670-A-G
• gnomAD v4: 22-42127668-A-G
• MyVariant Identifiers: chr22:g.42523670A>G (hg19) ; chr22:g.42127668A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42127668A>G , CM000684.2:g.42127668A>G	GRCh38
NC_000022.10:g.42523670A>G , CM000684.1:g.42523670A>G	GRCh37
NC_000022.9:g.40853614A>G	NCBI36
NG_008376.3:g.7324T>C
NG_008376.4:g.8143T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.784-34T>C	ENSP00000353241.6:n.784-34T>C
ENST00000645361.2:c.986-34T>C MANE Select	ENSP00000496150.1:n.986-34T>C
ENST00000359033.4:c.833-34T>C	ENSP00000351927.4:n.833-34T>C
ENST00000360124.9:c.604-34T>C	ENSP00000353241.5:n.604-34T>C
ENST00000360608.9:c.986-34T>C	ENSP00000353820.5:n.986-34T>C
ENST00000389970.7:c.949-6T>C	ENSP00000374620.4:n.949-6T>C
ENST00000488442.1:n.1710-34T>C
NM_000106.5:c.986-34T>C	NP_000097.3:n.986-34T>C
NM_001025161.2:c.833-34T>C	NP_001020332.2:n.833-34T>C
XM_011529966.1:c.986-34T>C	XP_011528268.1:n.986-34T>C
XM_011529967.1:c.986-34T>C	XP_011528269.1:n.986-34T>C
XM_011529968.1:c.986-34T>C	XP_011528270.1:n.986-34T>C
XM_011529969.1:c.842-34T>C	XP_011528271.1:n.842-34T>C
XM_011529970.1:c.833-34T>C	XP_011528272.1:n.833-34T>C
XM_011529971.1:c.842-34T>C	XP_011528273.1:n.842-34T>C
XM_011529972.1:c.844-34T>C	XP_011528274.1:n.844-34T>C
NM_000106.6:c.986-34T>C MANE Select	NP_000097.3:n.986-34T>C
NM_001025161.3:c.833-34T>C	NP_001020332.2:n.833-34T>C