Canonical Allele Identifier: CA2187826922

Gene: CYP1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74754548C= , CM000677.2:g.74754548C=	GRCh38
NC_000015.9:g.75046889C= , CM000677.1:g.75046889C=	GRCh37
NC_000015.8:g.72833942C=	NCBI36
NG_008431.1:g.37007C=
NG_008431.2:g.37007C=
NG_061543.1:g.10704C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343932.5:c.1254-243C= MANE Select	ENSP00000342007.4:n.1254-243C=
ENST00000343932.4:c.1254-243C=	ENSP00000342007.4:n.1254-243C=
NM_000761.4:c.1254-243C=	NP_000752.2:n.1254-243C=
NM_000761.5:c.1254-243C= MANE Select	NP_000752.2:n.1254-243C=