Canonical Allele Identifier: CA2819058998

Gene: CYP2D7

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42142321T>C , CM000684.2:g.42142321T>C	GRCh38
NC_000022.10:g.42538331T>C , CM000684.1:g.42538331T>C	GRCh37
NC_000022.9:g.40868275T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000651010.1:n.2620+158A>G
ENST00000358097.8:c.667+158A>G	ENSP00000445124.1:n.667+158A>G
ENST00000433992.2:c.667+158A>G	ENSP00000439604.1:n.667+158A>G
ENST00000610593.4:n.752+158A>G
ENST00000612115.1:c.666+158A>G	ENSP00000484065.1:n.666+158A>G
ENST00000614967.4:c.513+158A>G	ENSP00000481168.1:n.513+158A>G
NR_002570.3:n.778+158A>G
NM_001348386.2:c.666+158A>G	NP_001335315.1:n.666+158A>G
NR_002570.5:n.686+158A>G
NR_145674.2:n.686+158A>G
NM_001348386.3:c.666+158A>G	NP_001335315.1:n.666+158A>G
NR_002570.6:n.686+158A>G
NR_145674.3:n.686+158A>G