Canonical Allele Identifier: CA2187824668
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749960C= , CM000677.2:g.74749960C= GRCh38
NC_000015.9:g.75042301C= , CM000677.1:g.75042301C= GRCh37
NC_000015.8:g.72829354C= NCBI36
NG_008431.1:g.32419C=
NG_008431.2:g.32419C=
NG_061543.1:g.6116C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.222C= MANE Select ENSP00000342007.4:p.Asp74=
ENST00000343932.4:c.222C= ENSP00000342007.4:p.Asp74=
NM_000761.4:c.222C= NP_000752.2:p.Asp74=
NM_000761.5:c.222C= MANE Select NP_000752.2:p.Asp74=