Canonical Allele Identifier: CA2187824796
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74750230T= , CM000677.2:g.74750230T= GRCh38
NC_000015.9:g.75042571T= , CM000677.1:g.75042571T= GRCh37
NC_000015.8:g.72829624T= NCBI36
NG_008431.1:g.32689T=
NG_008431.2:g.32689T=
NG_061543.1:g.6386T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.492T= MANE Select ENSP00000342007.4:p.His164=
ENST00000343932.4:c.492T= ENSP00000342007.4:p.His164=
NM_000761.4:c.492T= NP_000752.2:p.His164=
NM_000761.5:c.492T= MANE Select NP_000752.2:p.His164=