Canonical Allele Identifier: CA2187824582
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749776A= , CM000677.2:g.74749776A= GRCh38
NC_000015.9:g.75042117A= , CM000677.1:g.75042117A= GRCh37
NC_000015.8:g.72829170A= NCBI36
NG_008431.1:g.32235A=
NG_008431.2:g.32235A=
NG_061543.1:g.5932A=

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.38A= MANE Select ENSP00000342007.4:p.Glu13=
ENST00000343932.4:c.38A= ENSP00000342007.4:p.Glu13=
NM_000761.4:c.38A= NP_000752.2:p.Glu13=
NM_000761.5:c.38A= MANE Select NP_000752.2:p.Glu13=