Canonical Allele Identifier: CA2406586621
Gene: CYP2D7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42142312T= , CM000684.2:g.42142312T= GRCh38
NC_000022.10:g.42538322T= , CM000684.1:g.42538322T= GRCh37
NC_000022.9:g.40868266T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000651010.1:n.2620+167A=
ENST00000358097.8:c.667+167A= ENSP00000445124.1:n.667+167A=
ENST00000433992.2:c.667+167A= ENSP00000439604.1:n.667+167A=
ENST00000610593.4:n.752+167A=
ENST00000612115.1:c.666+167A= ENSP00000484065.1:n.666+167A=
ENST00000614967.4:c.513+167A= ENSP00000481168.1:n.513+167A=
NR_002570.3:n.778+167A=
NM_001348386.2:c.666+167A= NP_001335315.1:n.666+167A=
NR_002570.5:n.686+167A=
NR_145674.2:n.686+167A=
NM_001348386.3:c.666+167A= NP_001335315.1:n.666+167A=
NR_002570.6:n.686+167A=
NR_145674.3:n.686+167A=