Canonical Allele Identifier: CA10264839
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs764713786

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42128154A>G , CM000684.2:g.42128154A>G GRCh38
NC_000022.10:g.42524156A>G , CM000684.1:g.42524156A>G GRCh37
NC_000022.9:g.40854100A>G NCBI36
NG_008376.3:g.6838T>C
NG_008376.4:g.7657T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000360124.10:c.690+20T>C ENSP00000353241.6:n.690+20T>C
ENST00000645361.2:c.843+20T>C MANE Select ENSP00000496150.1:n.843+20T>C
ENST00000359033.4:c.690+20T>C ENSP00000351927.4:n.690+20T>C
ENST00000360124.9:c.510+20T>C ENSP00000353241.5:n.510+20T>C
ENST00000360608.9:c.843+20T>C ENSP00000353820.5:n.843+20T>C
ENST00000389970.7:c.777+20T>C ENSP00000374620.4:n.777+20T>C
ENST00000488442.1:n.1567+20T>C
NM_000106.5:c.843+20T>C NP_000097.3:n.843+20T>C
NM_001025161.2:c.690+20T>C NP_001020332.2:n.690+20T>C
XM_011529966.1:c.843+20T>C XP_011528268.1:n.843+20T>C
XM_011529967.1:c.843+20T>C XP_011528269.1:n.843+20T>C
XM_011529968.1:c.843+20T>C XP_011528270.1:n.843+20T>C
XM_011529969.1:c.699+20T>C XP_011528271.1:n.699+20T>C
XM_011529970.1:c.690+20T>C XP_011528272.1:n.690+20T>C
XM_011529971.1:c.699+20T>C XP_011528273.1:n.699+20T>C
XM_011529972.1:c.843+20T>C XP_011528274.1:n.843+20T>C
NM_000106.6:c.843+20T>C MANE Select NP_000097.3:n.843+20T>C
NM_001025161.3:c.690+20T>C NP_001020332.2:n.690+20T>C