Canonical Allele Identifier: CA2406585677
Community Standard Title: NC_000022.11:g.42140943A=
Gene: CYP2D7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42140943A= , CM000684.2:g.42140943A= GRCh38
NC_000022.10:g.42536954A= , CM000684.1:g.42536954A= GRCh37
NC_000022.9:g.40866898A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001348386.2:c.1230+209T= NP_001335315.1:n.1230+209T=
NM_001348386.3:c.1230+209T= NP_001335315.1:n.1230+209T=
NR_002570.3:n.1285+209T=
NR_002570.5:n.1193+209T=
NR_002570.6:n.1193+209T=
NR_145674.2:n.1250+209T=
NR_145674.3:n.1250+209T=
ENST00000358097.8:c.1174+209T= ENSP00000445124.1:n.1174+209T=
ENST00000433992.2:c.1231+209T= ENSP00000439604.1:n.1231+209T=
ENST00000435101.1:c.296+209T= ENSP00000437680.2:n.296+209T=
ENST00000435101.2:n.296+209T=
ENST00000612115.1:c.1227+209T= ENSP00000484065.1:n.1227+209T=
ENST00000614967.4:c.1020+209T= ENSP00000481168.1:n.1020+209T=
ENST00000651010.1:n.3149+209T=