Canonical Allele Identifier: CA1025921880

Gene: CYP2D7

Linked Data

• dbSNP Id: rs1243949613
• gnomAD v3: 22-42142314-T-C
• gnomAD v4: 22-42142314-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42142314T>C , CM000684.2:g.42142314T>C	GRCh38
NC_000022.10:g.42538324T>C , CM000684.1:g.42538324T>C	GRCh37
NC_000022.9:g.40868268T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000651010.1:n.2620+165A>G
ENST00000358097.8:c.667+165A>G	ENSP00000445124.1:n.667+165A>G
ENST00000433992.2:c.667+165A>G	ENSP00000439604.1:n.667+165A>G
ENST00000610593.4:n.752+165A>G
ENST00000612115.1:c.666+165A>G	ENSP00000484065.1:n.666+165A>G
ENST00000614967.4:c.513+165A>G	ENSP00000481168.1:n.513+165A>G
NR_002570.3:n.778+165A>G
NM_001348386.2:c.666+165A>G	NP_001335315.1:n.666+165A>G
NR_002570.5:n.686+165A>G
NR_145674.2:n.686+165A>G
NM_001348386.3:c.666+165A>G	NP_001335315.1:n.666+165A>G
NR_002570.6:n.686+165A>G
NR_145674.3:n.686+165A>G