Canonical Allele Identifier: CA2187824439
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749426A= , CM000677.2:g.74749426A= GRCh38
NC_000015.9:g.75041767A= , CM000677.1:g.75041767A= GRCh37
NC_000015.8:g.72828820A= NCBI36
NG_008431.1:g.31885A=
NG_008431.2:g.31885A=
NG_061543.1:g.5582A=

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.-9-304A= MANE Select ENSP00000342007.4:n.-9-304A=
ENST00000343932.4:c.-9-304A= ENSP00000342007.4:n.-9-304A=
NM_000761.4:c.-9-304A= NP_000752.2:n.-9-304A=
NM_000761.5:c.-9-304A= MANE Select NP_000752.2:n.-9-304A=