Canonical Allele Identifier: CA2187824484
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749533A= , CM000677.2:g.74749533A= GRCh38
NC_000015.9:g.75041874A= , CM000677.1:g.75041874A= GRCh37
NC_000015.8:g.72828927A= NCBI36
NG_008431.1:g.31992A=
NG_008431.2:g.31992A=
NG_061543.1:g.5689A=

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.-9-197A= MANE Select ENSP00000342007.4:n.-9-197A=
ENST00000343932.4:c.-9-197A= ENSP00000342007.4:n.-9-197A=
NM_000761.4:c.-9-197A= NP_000752.2:n.-9-197A=
NM_000761.5:c.-9-197A= MANE Select NP_000752.2:n.-9-197A=