Canonical Allele Identifier: CA2187824555
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749708G= , CM000677.2:g.74749708G= GRCh38
NC_000015.9:g.75042049G= , CM000677.1:g.75042049G= GRCh37
NC_000015.8:g.72829102G= NCBI36
NG_008431.1:g.32167G=
NG_008431.2:g.32167G=
NG_061543.1:g.5864G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.-9-22G= MANE Select ENSP00000342007.4:n.-9-22G=
ENST00000343932.4:c.-9-22G= ENSP00000342007.4:n.-9-22G=
NM_000761.4:c.-9-22G= NP_000752.2:n.-9-22G=
NM_000761.5:c.-9-22G= MANE Select NP_000752.2:n.-9-22G=