Canonical Allele Identifier: CA2187824594

Gene: CYP1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74749801C= , CM000677.2:g.74749801C=	GRCh38
NC_000015.9:g.75042142C= , CM000677.1:g.75042142C=	GRCh37
NC_000015.8:g.72829195C=	NCBI36
NG_008431.1:g.32260C=
NG_008431.2:g.32260C=
NG_061543.1:g.5957C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000343932.5:c.63C= MANE Select	ENSP00000342007.4:p.Phe21=
ENST00000343932.4:c.63C=	ENSP00000342007.4:p.Phe21=
NM_000761.4:c.63C=	NP_000752.2:p.Phe21=
NM_000761.5:c.63C= MANE Select	NP_000752.2:p.Phe21=