Canonical Allele Identifier: CA2187827250
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755241G= , CM000677.2:g.74755241G= GRCh38
NC_000015.9:g.75047582G= , CM000677.1:g.75047582G= GRCh37
NC_000015.8:g.72834635G= NCBI36
NG_008431.1:g.37700G=
NG_008431.2:g.37700G=
NG_061543.1:g.11397G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*153G= MANE Select ENSP00000342007.4:n.*153G=
ENST00000343932.4:c.*153G= ENSP00000342007.4:n.*153G=
NM_000761.4:c.*153G= NP_000752.2:n.*153G=
NM_000761.5:c.*153G= MANE Select NP_000752.2:n.*153G=