Canonical Allele Identifier: CA2657038991
Community Standard Title: NC_000022.11:g.42143726G>C
Gene: CYP2D7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42143726G>C , CM000684.2:g.42143726G>C GRCh38
NC_000022.10:g.42539727G>C , CM000684.1:g.42539727G>C GRCh37
NC_000022.9:g.40869671G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001348386.2:c.181-145C>G NP_001335315.1:n.181-145C>G
NM_001348386.3:c.181-145C>G NP_001335315.1:n.181-145C>G
NR_002570.3:n.293-145C>G
NR_002570.5:n.201-145C>G
NR_002570.6:n.201-145C>G
NR_145674.2:n.201-145C>G
NR_145674.3:n.201-145C>G
ENST00000358097.8:c.182-145C>G ENSP00000445124.1:n.182-145C>G
ENST00000424775.1:n.257+17C>G
ENST00000433992.2:c.182-145C>G ENSP00000439604.1:n.182-145C>G
ENST00000435688.1:n.267-145C>G
ENST00000610593.4:n.267-145C>G
ENST00000612115.1:c.181-145C>G ENSP00000484065.1:n.181-145C>G
ENST00000614967.4:c.181-145C>G ENSP00000481168.1:n.181-145C>G
ENST00000651010.1:n.1990C>G