Canonical Allele Identifier: CA2406586651
Gene: CYP2D7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42142362T= , CM000684.2:g.42142362T= GRCh38
NC_000022.10:g.42538372T= , CM000684.1:g.42538372T= GRCh37
NC_000022.9:g.40868316T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651010.1:n.2620+117A=
ENST00000358097.8:c.667+117A= ENSP00000445124.1:n.667+117A=
ENST00000433992.2:c.667+117A= ENSP00000439604.1:n.667+117A=
ENST00000610593.4:n.752+117A=
ENST00000612115.1:c.666+117A= ENSP00000484065.1:n.666+117A=
ENST00000614967.4:c.513+117A= ENSP00000481168.1:n.513+117A=
NR_002570.3:n.778+117A=
NM_001348386.2:c.666+117A= NP_001335315.1:n.666+117A=
NR_002570.5:n.686+117A=
NR_145674.2:n.686+117A=
NM_001348386.3:c.666+117A= NP_001335315.1:n.666+117A=
NR_002570.6:n.686+117A=
NR_145674.3:n.686+117A=