Canonical Allele Identifier: CA2187824501
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749576C= , CM000677.2:g.74749576C= GRCh38
NC_000015.9:g.75041917C= , CM000677.1:g.75041917C= GRCh37
NC_000015.8:g.72828970C= NCBI36
NG_008431.1:g.32035C=
NG_008431.2:g.32035C=
NG_061543.1:g.5732C=

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.-9-154C= MANE Select ENSP00000342007.4:p.=
ENST00000343932.4:c.-9-154C= ENSP00000342007.4:p.=
NM_000761.4:c.-9-154C= NP_000752.2:p.=
NM_000761.5:c.-9-154C= MANE Select NP_000752.2:p.=