Canonical Allele Identifier: CA2406586628
Gene: CYP2D7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42142330C= , CM000684.2:g.42142330C= GRCh38
NC_000022.10:g.42538340C= , CM000684.1:g.42538340C= GRCh37
NC_000022.9:g.40868284C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651010.1:n.2620+149G=
ENST00000358097.8:c.667+149G= ENSP00000445124.1:n.667+149G=
ENST00000433992.2:c.667+149G= ENSP00000439604.1:n.667+149G=
ENST00000610593.4:n.752+149G=
ENST00000612115.1:c.666+149G= ENSP00000484065.1:n.666+149G=
ENST00000614967.4:c.513+149G= ENSP00000481168.1:n.513+149G=
NR_002570.3:n.778+149G=
NM_001348386.2:c.666+149G= NP_001335315.1:n.666+149G=
NR_002570.5:n.686+149G=
NR_145674.2:n.686+149G=
NM_001348386.3:c.666+149G= NP_001335315.1:n.666+149G=
NR_002570.6:n.686+149G=
NR_145674.3:n.686+149G=