Canonical Allele Identifier: CA2187824591
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749793G= , CM000677.2:g.74749793G= GRCh38
NC_000015.9:g.75042134G= , CM000677.1:g.75042134G= GRCh37
NC_000015.8:g.72829187G= NCBI36
NG_008431.1:g.32252G=
NG_008431.2:g.32252G=
NG_061543.1:g.5949G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.55G= MANE Select ENSP00000342007.4:p.Ala19=
ENST00000343932.4:c.55G= ENSP00000342007.4:p.Ala19=
NM_000761.4:c.55G= NP_000752.2:p.Ala19=
NM_000761.5:c.55G= MANE Select NP_000752.2:p.Ala19=