Canonical Allele Identifier: CA2804766390

Gene: CYP1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74755369A>T , CM000677.2:g.74755369A>T	GRCh38
NC_000015.9:g.75047710A>T , CM000677.1:g.75047710A>T	GRCh37
NC_000015.8:g.72834763A>T	NCBI36
NG_008431.1:g.37828A>T
NG_008431.2:g.37828A>T
NG_061543.1:g.11525A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343932.5:c.*281A>T MANE Select	ENSP00000342007.4:n.*281A>T
ENST00000343932.4:c.*281A>T	ENSP00000342007.4:n.*281A>T
NM_000761.4:c.*281A>T	NP_000752.2:n.*281A>T
NM_000761.5:c.*281A>T MANE Select	NP_000752.2:n.*281A>T