Canonical Allele Identifier: CA2406586655
Gene: CYP2D7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42142365A= , CM000684.2:g.42142365A= GRCh38
NC_000022.10:g.42538375A= , CM000684.1:g.42538375A= GRCh37
NC_000022.9:g.40868319A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651010.1:n.2620+114T=
ENST00000358097.8:c.667+114T= ENSP00000445124.1:n.667+114T=
ENST00000433992.2:c.667+114T= ENSP00000439604.1:n.667+114T=
ENST00000610593.4:n.752+114T=
ENST00000612115.1:c.666+114T= ENSP00000484065.1:n.666+114T=
ENST00000614967.4:c.513+114T= ENSP00000481168.1:n.513+114T=
NR_002570.3:n.778+114T=
NM_001348386.2:c.666+114T= NP_001335315.1:n.666+114T=
NR_002570.5:n.686+114T=
NR_145674.2:n.686+114T=
NM_001348386.3:c.666+114T= NP_001335315.1:n.666+114T=
NR_002570.6:n.686+114T=
NR_145674.3:n.686+114T=