Canonical Allele Identifier: CA2187824206

Gene: CYP1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74748907T= , CM000677.2:g.74748907T=	GRCh38
NC_000015.9:g.75041248T= , CM000677.1:g.75041248T=	GRCh37
NC_000015.8:g.72828301T=	NCBI36
NG_008431.1:g.31366T=
NG_008431.2:g.31366T=
NG_061543.1:g.5063T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343932.5:c.-10+10T= MANE Select	ENSP00000342007.4:n.-10+10T=
ENST00000343932.4:c.-10+10T=	ENSP00000342007.4:n.-10+10T=
NM_000761.4:c.-10+10T=	NP_000752.2:n.-10+10T=
NM_000761.5:c.-10+10T= MANE Select	NP_000752.2:n.-10+10T=