Canonical Allele Identifier: CA2657035465
Gene: CYP2D7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42142369T>C , CM000684.2:g.42142369T>C GRCh38
NC_000022.10:g.42538379T>C , CM000684.1:g.42538379T>C GRCh37
NC_000022.9:g.40868323T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651010.1:n.2620+110A>G
ENST00000358097.8:c.667+110A>G ENSP00000445124.1:n.667+110A>G
ENST00000433992.2:c.667+110A>G ENSP00000439604.1:n.667+110A>G
ENST00000610593.4:n.752+110A>G
ENST00000612115.1:c.666+110A>G ENSP00000484065.1:n.666+110A>G
ENST00000614967.4:c.513+110A>G ENSP00000481168.1:n.513+110A>G
NR_002570.3:n.778+110A>G
NM_001348386.2:c.666+110A>G NP_001335315.1:n.666+110A>G
NR_002570.5:n.686+110A>G
NR_145674.2:n.686+110A>G
NM_001348386.3:c.666+110A>G NP_001335315.1:n.666+110A>G
NR_002570.6:n.686+110A>G
NR_145674.3:n.686+110A>G