Canonical Allele Identifier: CA753340466

Gene: CYP2D7

Linked Data

• dbSNP Id: rs1192721965
• gnomAD v3: 22-42142404-T-TA
• gnomAD v4: 22-42142404-T-TA
• MyVariant Identifiers: chr22:g.42142404_42142405insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42142404_42142405insA , CM000684.2:g.42142404_42142405insA	GRCh38
NC_000022.10:g.42538414_42538415insA , CM000684.1:g.42538414_42538415insA	GRCh37
NC_000022.9:g.40868358_40868359insA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651010.1:n.2620+74_2620+75insT
ENST00000358097.8:c.667+74_667+75insT	ENSP00000445124.1:n.667+74_667+75insT
ENST00000433992.2:c.667+74_667+75insT	ENSP00000439604.1:n.667+74_667+75insT
ENST00000610593.4:n.752+74_752+75insT
ENST00000612115.1:c.666+74_666+75insT	ENSP00000484065.1:n.666+74_666+75insT
ENST00000614967.4:c.513+74_513+75insT	ENSP00000481168.1:n.513+74_513+75insT
NR_002570.3:n.778+74_778+75insT
NM_001348386.2:c.666+74_666+75insT	NP_001335315.1:n.666+74_666+75insT
NR_002570.5:n.686+74_686+75insT
NR_145674.2:n.686+74_686+75insT
NM_001348386.3:c.666+74_666+75insT	NP_001335315.1:n.666+74_666+75insT
NR_002570.6:n.686+74_686+75insT
NR_145674.3:n.686+74_686+75insT