Canonical Allele Identifier: CA639828130

Gene: CYP2D7

Linked Data

• dbSNP Id: rs951521050
• gnomAD v2: 22-42538334-C-G
• gnomAD v3: 22-42142324-C-G
• gnomAD v4: 22-42142324-C-G
• MyVariant Identifiers: chr22:g.42538334C>G (hg19) ; chr22:g.42142324C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42142324C>G , CM000684.2:g.42142324C>G	GRCh38
NC_000022.10:g.42538334C>G , CM000684.1:g.42538334C>G	GRCh37
NC_000022.9:g.40868278C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000651010.1:n.2620+155G>C
ENST00000358097.8:c.667+155G>C	ENSP00000445124.1:n.667+155G>C
ENST00000433992.2:c.667+155G>C	ENSP00000439604.1:n.667+155G>C
ENST00000610593.4:n.752+155G>C
ENST00000612115.1:c.666+155G>C	ENSP00000484065.1:n.666+155G>C
ENST00000614967.4:c.513+155G>C	ENSP00000481168.1:n.513+155G>C
NR_002570.3:n.778+155G>C
NM_001348386.2:c.666+155G>C	NP_001335315.1:n.666+155G>C
NR_002570.5:n.686+155G>C
NR_145674.2:n.686+155G>C
NM_001348386.3:c.666+155G>C	NP_001335315.1:n.666+155G>C
NR_002570.6:n.686+155G>C
NR_145674.3:n.686+155G>C