Canonical Allele Identifier: CA2187824521
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749625G= , CM000677.2:g.74749625G= GRCh38
NC_000015.9:g.75041966G= , CM000677.1:g.75041966G= GRCh37
NC_000015.8:g.72829019G= NCBI36
NG_008431.1:g.32084G=
NG_008431.2:g.32084G=
NG_061543.1:g.5781G=

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.-9-105G= MANE Select ENSP00000342007.4:p.=
ENST00000343932.4:c.-9-105G= ENSP00000342007.4:p.=
NM_000761.4:c.-9-105G= NP_000752.2:p.=
NM_000761.5:c.-9-105G= MANE Select NP_000752.2:p.=