Canonical Allele Identifier: CA1025921938
Gene: CYP2D7 HGNC NCBI

Linked Data

dbSNP Id: rs1934329250
gnomAD v3: 22-42142364-G-T
gnomAD v4: 22-42142364-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42142364G>T , CM000684.2:g.42142364G>T GRCh38
NC_000022.10:g.42538374G>T , CM000684.1:g.42538374G>T GRCh37
NC_000022.9:g.40868318G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651010.1:n.2620+115C>A
ENST00000358097.8:c.667+115C>A ENSP00000445124.1:n.667+115C>A
ENST00000433992.2:c.667+115C>A ENSP00000439604.1:n.667+115C>A
ENST00000610593.4:n.752+115C>A
ENST00000612115.1:c.666+115C>A ENSP00000484065.1:n.666+115C>A
ENST00000614967.4:c.513+115C>A ENSP00000481168.1:n.513+115C>A
NR_002570.3:n.778+115C>A
NM_001348386.2:c.666+115C>A NP_001335315.1:n.666+115C>A
NR_002570.5:n.686+115C>A
NR_145674.2:n.686+115C>A
NM_001348386.3:c.666+115C>A NP_001335315.1:n.666+115C>A
NR_002570.6:n.686+115C>A
NR_145674.3:n.686+115C>A
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