Canonical Allele Identifier: CA411773526
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs190535395

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42128300C>G , CM000684.2:g.42128300C>G GRCh38
NC_000022.10:g.42524302C>G , CM000684.1:g.42524302C>G GRCh37
NC_000022.9:g.40854246C>G NCBI36
NG_008376.3:g.6692G>C
NG_008376.4:g.7511G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000360124.10:c.564G>C ENSP00000353241.6:p.Lys188Asn
ENST00000645361.2:c.717G>C MANE Select ENSP00000496150.1:p.Lys239Asn
ENST00000359033.4:c.564G>C ENSP00000351927.4:p.Lys188Asn
ENST00000360124.9:c.384G>C ENSP00000353241.5:p.Lys128Asn
ENST00000360608.9:c.717G>C ENSP00000353820.5:p.Lys239Asn
ENST00000389970.7:c.651G>C ENSP00000374620.4:p.Lys217Asn
ENST00000488442.1:n.1441G>C
NM_000106.5:c.717G>C NP_000097.3:p.Lys239Asn
NM_001025161.2:c.564G>C NP_001020332.2:p.Lys188Asn
XM_011529966.1:c.717G>C XP_011528268.1:p.Lys239Asn
XM_011529967.1:c.717G>C XP_011528269.1:p.Lys239Asn
XM_011529968.1:c.717G>C XP_011528270.1:p.Lys239Asn
XM_011529969.1:c.573G>C XP_011528271.1:p.Lys191Asn
XM_011529970.1:c.564G>C XP_011528272.1:p.Lys188Asn
XM_011529971.1:c.573G>C XP_011528273.1:p.Lys191Asn
XM_011529972.1:c.717G>C XP_011528274.1:p.Lys239Asn
NM_000106.6:c.717G>C MANE Select NP_000097.3:p.Lys239Asn
NM_001025161.3:c.564G>C NP_001020332.2:p.Lys188Asn