Canonical Allele Identifier: CA2738249490

Gene: CYP2D6

Linked Data

• dbSNP Id: rs2146932301

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42127767T>C , CM000684.2:g.42127767T>C	GRCh38
NC_000022.10:g.42523769T>C , CM000684.1:g.42523769T>C	GRCh37
NC_000022.9:g.40853713T>C	NCBI36
NG_008376.3:g.7225A>G
NG_008376.4:g.8044A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.783+75A>G	ENSP00000353241.6:n.783+75A>G
ENST00000645361.2:c.985+75A>G MANE Select	ENSP00000496150.1:n.985+75A>G
ENST00000359033.4:c.832+75A>G	ENSP00000351927.4:n.832+75A>G
ENST00000360124.9:c.603+75A>G	ENSP00000353241.5:n.603+75A>G
ENST00000360608.9:c.985+75A>G	ENSP00000353820.5:n.985+75A>G
ENST00000389970.7:c.948+14A>G	ENSP00000374620.4:n.948+14A>G
ENST00000488442.1:n.1709+75A>G
NM_000106.5:c.985+75A>G	NP_000097.3:n.985+75A>G
NM_001025161.2:c.832+75A>G	NP_001020332.2:n.832+75A>G
XM_011529966.1:c.985+75A>G	XP_011528268.1:n.985+75A>G
XM_011529967.1:c.985+75A>G	XP_011528269.1:n.985+75A>G
XM_011529968.1:c.985+75A>G	XP_011528270.1:n.985+75A>G
XM_011529969.1:c.841+75A>G	XP_011528271.1:n.841+75A>G
XM_011529970.1:c.832+75A>G	XP_011528272.1:n.832+75A>G
XM_011529971.1:c.841+75A>G	XP_011528273.1:n.841+75A>G
XM_011529972.1:c.844-133A>G	XP_011528274.1:n.844-133A>G
NM_000106.6:c.985+75A>G MANE Select	NP_000097.3:n.985+75A>G
NM_001025161.3:c.832+75A>G	NP_001020332.2:n.832+75A>G