Canonical Allele Identifier: CA2738160204
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs1414056715

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42127772G>C , CM000684.2:g.42127772G>C GRCh38
NC_000022.10:g.42523774G>C , CM000684.1:g.42523774G>C GRCh37
NC_000022.9:g.40853718G>C NCBI36
NG_008376.3:g.7220C>G
NG_008376.4:g.8039C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360124.10:c.783+70C>G ENSP00000353241.6:n.783+70C>G
ENST00000645361.2:c.985+70C>G MANE Select ENSP00000496150.1:n.985+70C>G
ENST00000359033.4:c.832+70C>G ENSP00000351927.4:n.832+70C>G
ENST00000360124.9:c.603+70C>G ENSP00000353241.5:n.603+70C>G
ENST00000360608.9:c.985+70C>G ENSP00000353820.5:n.985+70C>G
ENST00000389970.7:c.948+9C>G ENSP00000374620.4:n.948+9C>G
ENST00000488442.1:n.1709+70C>G
NM_000106.5:c.985+70C>G NP_000097.3:n.985+70C>G
NM_001025161.2:c.832+70C>G NP_001020332.2:n.832+70C>G
XM_011529966.1:c.985+70C>G XP_011528268.1:n.985+70C>G
XM_011529967.1:c.985+70C>G XP_011528269.1:n.985+70C>G
XM_011529968.1:c.985+70C>G XP_011528270.1:n.985+70C>G
XM_011529969.1:c.841+70C>G XP_011528271.1:n.841+70C>G
XM_011529970.1:c.832+70C>G XP_011528272.1:n.832+70C>G
XM_011529971.1:c.841+70C>G XP_011528273.1:n.841+70C>G
XM_011529972.1:c.844-138C>G XP_011528274.1:n.844-138C>G
NM_000106.6:c.985+70C>G MANE Select NP_000097.3:n.985+70C>G
NM_001025161.3:c.832+70C>G NP_001020332.2:n.832+70C>G