Canonical Allele Identifier: CA411772142

Gene: CYP2D6

Linked Data

• dbSNP Id: rs2146931971
• MyVariant Identifiers: chr22:g.42523665T>C (hg19) ; chr22:g.42127663T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42127663T>C , CM000684.2:g.42127663T>C	GRCh38
NC_000022.10:g.42523665T>C , CM000684.1:g.42523665T>C	GRCh37
NC_000022.9:g.40853609T>C	NCBI36
NG_008376.3:g.7329A>G
NG_008376.4:g.8148A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.784-29A>G	ENSP00000353241.6:n.784-29A>G
ENST00000645361.2:c.986-29A>G MANE Select	ENSP00000496150.1:n.986-29A>G
ENST00000359033.4:c.833-29A>G	ENSP00000351927.4:n.833-29A>G
ENST00000360124.9:c.604-29A>G	ENSP00000353241.5:n.604-29A>G
ENST00000360608.9:c.986-29A>G	ENSP00000353820.5:n.986-29A>G
ENST00000389970.7:c.949-1A>G	ENSP00000374620.4:n.949-1A>G
ENST00000488442.1:n.1710-29A>G
NM_000106.5:c.986-29A>G	NP_000097.3:n.986-29A>G
NM_001025161.2:c.833-29A>G	NP_001020332.2:n.833-29A>G
XM_011529966.1:c.986-29A>G	XP_011528268.1:n.986-29A>G
XM_011529967.1:c.986-29A>G	XP_011528269.1:n.986-29A>G
XM_011529968.1:c.986-29A>G	XP_011528270.1:n.986-29A>G
XM_011529969.1:c.842-29A>G	XP_011528271.1:n.842-29A>G
XM_011529970.1:c.833-29A>G	XP_011528272.1:n.833-29A>G
XM_011529971.1:c.842-29A>G	XP_011528273.1:n.842-29A>G
XM_011529972.1:c.844-29A>G	XP_011528274.1:n.844-29A>G
NM_000106.6:c.986-29A>G MANE Select	NP_000097.3:n.986-29A>G
NM_001025161.3:c.833-29A>G	NP_001020332.2:n.833-29A>G