Canonical Allele Identifier: CA2836570286

Gene: CYP1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74748865A>G , CM000677.2:g.74748865A>G	GRCh38
NC_000015.9:g.75041206A>G , CM000677.1:g.75041206A>G	GRCh37
NC_000015.8:g.72828259A>G	NCBI36
NG_008431.1:g.31324A>G
NG_008431.2:g.31324A>G
NG_061543.1:g.5021A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343932.5:c.-42A>G MANE Select	ENSP00000342007.4:n.-42A>G
ENST00000343932.4:c.-42A>G	ENSP00000342007.4:n.-42A>G
NM_000761.4:c.-42A>G	NP_000752.2:n.-42A>G
NM_000761.5:c.-42A>G MANE Select	NP_000752.2:n.-42A>G