Canonical Allele Identifier: CA2657035556
Gene: CYP2D7 HGNC NCBI

Linked Data

gnomAD v4: 22-42142415-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42142415A>C , CM000684.2:g.42142415A>C GRCh38
NC_000022.10:g.42538425A>C , CM000684.1:g.42538425A>C GRCh37
NC_000022.9:g.40868369A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000651010.1:n.2620+64T>G
ENST00000358097.8:c.667+64T>G ENSP00000445124.1:n.667+64T>G
ENST00000433992.2:c.667+64T>G ENSP00000439604.1:n.667+64T>G
ENST00000610593.4:n.752+64T>G
ENST00000612115.1:c.666+64T>G ENSP00000484065.1:n.666+64T>G
ENST00000614967.4:c.513+64T>G ENSP00000481168.1:n.513+64T>G
NR_002570.3:n.778+64T>G
NM_001348386.2:c.666+64T>G NP_001335315.1:n.666+64T>G
NR_002570.5:n.686+64T>G
NR_145674.2:n.686+64T>G
NM_001348386.3:c.666+64T>G NP_001335315.1:n.666+64T>G
NR_002570.6:n.686+64T>G
NR_145674.3:n.686+64T>G
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