Canonical Allele Identifier: CA753340338
Gene: CYP2D7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42142219A>C , CM000684.2:g.42142219A>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000651010.1:n.2621-175T>G
ENST00000358097.8:c.668-175T>G ENSP00000445124.1:n.668-175T>G
ENST00000433992.2:c.668-175T>G ENSP00000439604.1:n.668-175T>G
ENST00000610593.4:n.753-175T>G
ENST00000612115.1:c.667-175T>G ENSP00000484065.1:n.667-175T>G
ENST00000614967.4:c.514-175T>G ENSP00000481168.1:n.514-175T>G
NR_002570.3:n.779-175T>G
NM_001348386.2:c.667-175T>G NP_001335315.1:n.667-175T>G
NR_002570.5:n.687-175T>G
NR_145674.2:n.687-175T>G
NM_001348386.3:c.667-175T>G NP_001335315.1:n.667-175T>G
NR_002570.6:n.687-175T>G
NR_145674.3:n.687-175T>G