Canonical Allele Identifier: CA2187827213
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755129C= , CM000677.2:g.74755129C= GRCh38
NC_000015.9:g.75047470C= , CM000677.1:g.75047470C= GRCh37
NC_000015.8:g.72834523C= NCBI36
NG_008431.1:g.37588C=
NG_008431.2:g.37588C=
NG_061543.1:g.11285C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*41C= MANE Select ENSP00000342007.4:n.*41C=
ENST00000343932.4:c.*41C= ENSP00000342007.4:n.*41C=
NM_000761.4:c.*41C= NP_000752.2:n.*41C=
NM_000761.5:c.*41C= MANE Select NP_000752.2:n.*41C=