Canonical Allele Identifier: CA2187824596
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749804C= , CM000677.2:g.74749804C= GRCh38
NC_000015.9:g.75042145C= , CM000677.1:g.75042145C= GRCh37
NC_000015.8:g.72829198C= NCBI36
NG_008431.1:g.32263C=
NG_008431.2:g.32263C=
NG_061543.1:g.5960C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.66C= MANE Select ENSP00000342007.4:p.Cys22=
ENST00000343932.4:c.66C= ENSP00000342007.4:p.Cys22=
NM_000761.4:c.66C= NP_000752.2:p.Cys22=
NM_000761.5:c.66C= MANE Select NP_000752.2:p.Cys22=