Canonical Allele Identifier: CA2187824426
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749406G= , CM000677.2:g.74749406G= GRCh38
NC_000015.9:g.75041747G= , CM000677.1:g.75041747G= GRCh37
NC_000015.8:g.72828800G= NCBI36
NG_008431.1:g.31865G=
NG_008431.2:g.31865G=
NG_061543.1:g.5562G=

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.-9-324G= MANE Select ENSP00000342007.4:n.-9-324G=
ENST00000343932.4:c.-9-324G= ENSP00000342007.4:n.-9-324G=
NM_000761.4:c.-9-324G= NP_000752.2:n.-9-324G=
NM_000761.5:c.-9-324G= MANE Select NP_000752.2:n.-9-324G=