Canonical Allele Identifier: CA2406586652
Gene: CYP2D7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42142363G= , CM000684.2:g.42142363G= GRCh38
NC_000022.10:g.42538373G= , CM000684.1:g.42538373G= GRCh37
NC_000022.9:g.40868317G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651010.1:n.2620+116C=
ENST00000358097.8:c.667+116C= ENSP00000445124.1:n.667+116C=
ENST00000433992.2:c.667+116C= ENSP00000439604.1:n.667+116C=
ENST00000610593.4:n.752+116C=
ENST00000612115.1:c.666+116C= ENSP00000484065.1:n.666+116C=
ENST00000614967.4:c.513+116C= ENSP00000481168.1:n.513+116C=
NR_002570.3:n.778+116C=
NM_001348386.2:c.666+116C= NP_001335315.1:n.666+116C=
NR_002570.5:n.686+116C=
NR_145674.2:n.686+116C=
NM_001348386.3:c.666+116C= NP_001335315.1:n.666+116C=
NR_002570.6:n.686+116C=
NR_145674.3:n.686+116C=