Canonical Allele Identifier: CA2840394719

Gene: CYP1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74754778G>T , CM000677.2:g.74754778G>T	GRCh38
NC_000015.9:g.75047119G>T , CM000677.1:g.75047119G>T	GRCh37
NC_000015.8:g.72834172G>T	NCBI36
NG_008431.1:g.37237G>T
NG_008431.2:g.37237G>T
NG_061543.1:g.10934G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343932.5:c.1254-13G>T MANE Select	ENSP00000342007.4:n.1254-13G>T
ENST00000343932.4:c.1254-13G>T	ENSP00000342007.4:n.1254-13G>T
NM_000761.4:c.1254-13G>T	NP_000752.2:n.1254-13G>T
NM_000761.5:c.1254-13G>T MANE Select	NP_000752.2:n.1254-13G>T