Canonical Allele Identifier: CA2187824504
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749578A= , CM000677.2:g.74749578A= GRCh38
NC_000015.9:g.75041919A= , CM000677.1:g.75041919A= GRCh37
NC_000015.8:g.72828972A= NCBI36
NG_008431.1:g.32037A=
NG_008431.2:g.32037A=
NG_061543.1:g.5734A=

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.-9-152A= MANE Select ENSP00000342007.4:p.=
ENST00000343932.4:c.-9-152A= ENSP00000342007.4:p.=
NM_000761.4:c.-9-152A= NP_000752.2:p.=
NM_000761.5:c.-9-152A= MANE Select NP_000752.2:p.=