Canonical Allele Identifier: CA2187825724

Gene: CYP1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74752157T= , CM000677.2:g.74752157T=	GRCh38
NC_000015.9:g.75044498T= , CM000677.1:g.75044498T=	GRCh37
NC_000015.8:g.72831551T=	NCBI36
NG_008431.1:g.34616T=
NG_008431.2:g.34616T=
NG_061543.1:g.8313T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343932.5:c.1076T= MANE Select	ENSP00000342007.4:p.Leu359=
ENST00000343932.4:c.1076T=	ENSP00000342007.4:p.Leu359=
NM_000761.4:c.1076T=	NP_000752.2:p.Leu359=
NM_000761.5:c.1076T= MANE Select	NP_000752.2:p.Leu359=