Canonical Allele Identifier: CA2187824193
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74748875A= , CM000677.2:g.74748875A= GRCh38
NC_000015.9:g.75041216A= , CM000677.1:g.75041216A= GRCh37
NC_000015.8:g.72828269A= NCBI36
NG_008431.1:g.31334A=
NG_008431.2:g.31334A=
NG_061543.1:g.5031A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.-32A= MANE Select ENSP00000342007.4:n.-32A=
ENST00000343932.4:c.-32A= ENSP00000342007.4:n.-32A=
NM_000761.4:c.-32A= NP_000752.2:n.-32A=
NM_000761.5:c.-32A= MANE Select NP_000752.2:n.-32A=