Canonical Allele Identifier: CA2187824806

Gene: CYP1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74750259G= , CM000677.2:g.74750259G=	GRCh38
NC_000015.9:g.75042600G= , CM000677.1:g.75042600G=	GRCh37
NC_000015.8:g.72829653G=	NCBI36
NG_008431.1:g.32718G=
NG_008431.2:g.32718G=
NG_061543.1:g.6415G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343932.5:c.521G= MANE Select	ENSP00000342007.4:p.Ser174=
ENST00000343932.4:c.521G=	ENSP00000342007.4:p.Ser174=
NM_000761.4:c.521G=	NP_000752.2:p.Ser174=
NM_000761.5:c.521G= MANE Select	NP_000752.2:p.Ser174=