Canonical Allele Identifier: CA2657035408

Gene: CYP2D7

Linked Data

• gnomAD v4: 22-42142338-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42142338G>T , CM000684.2:g.42142338G>T	GRCh38
NC_000022.10:g.42538348G>T , CM000684.1:g.42538348G>T	GRCh37
NC_000022.9:g.40868292G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000651010.1:n.2620+141C>A
ENST00000358097.8:c.667+141C>A	ENSP00000445124.1:n.667+141C>A
ENST00000433992.2:c.667+141C>A	ENSP00000439604.1:n.667+141C>A
ENST00000610593.4:n.752+141C>A
ENST00000612115.1:c.666+141C>A	ENSP00000484065.1:n.666+141C>A
ENST00000614967.4:c.513+141C>A	ENSP00000481168.1:n.513+141C>A
NR_002570.3:n.778+141C>A
NM_001348386.2:c.666+141C>A	NP_001335315.1:n.666+141C>A
NR_002570.5:n.686+141C>A
NR_145674.2:n.686+141C>A
NM_001348386.3:c.666+141C>A	NP_001335315.1:n.666+141C>A
NR_002570.6:n.686+141C>A
NR_145674.3:n.686+141C>A