Canonical Allele Identifier: CA2187824670
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749963C= , CM000677.2:g.74749963C= GRCh38
NC_000015.9:g.75042304C= , CM000677.1:g.75042304C= GRCh37
NC_000015.8:g.72829357C= NCBI36
NG_008431.1:g.32422C=
NG_008431.2:g.32422C=
NG_061543.1:g.6119C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.225C= MANE Select ENSP00000342007.4:p.Val75=
ENST00000343932.4:c.225C= ENSP00000342007.4:p.Val75=
NM_000761.4:c.225C= NP_000752.2:p.Val75=
NM_000761.5:c.225C= MANE Select NP_000752.2:p.Val75=