Canonical Allele Identifier: CA2187827195
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755096A= , CM000677.2:g.74755096A= GRCh38
NC_000015.9:g.75047437A= , CM000677.1:g.75047437A= GRCh37
NC_000015.8:g.72834490A= NCBI36
NG_008431.1:g.37555A=
NG_008431.2:g.37555A=
NG_061543.1:g.11252A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*8A= MANE Select ENSP00000342007.4:n.*8A=
ENST00000343932.4:c.*8A= ENSP00000342007.4:n.*8A=
NM_000761.4:c.*8A= NP_000752.2:n.*8A=
NM_000761.5:c.*8A= MANE Select NP_000752.2:n.*8A=