Canonical Allele Identifier: CA971501126

Gene: CYP1A2

Linked Data

• dbSNP Id: rs1041862747
• gnomAD v3: 15-74755370-C-CAA
• gnomAD v4: 15-74755370-C-CAA

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74755379_74755380dup , CM000677.2:g.74755379_74755380dup	GRCh38
NC_000015.9:g.75047720_75047721dup , CM000677.1:g.75047720_75047721dup	GRCh37
NC_000015.8:g.72834773_72834774dup	NCBI36
NG_008431.1:g.37838_37839dup
NG_008431.2:g.37838_37839dup
NG_061543.1:g.11535_11536dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343932.5:c.*291_*292dup MANE Select	ENSP00000342007.4:n.*291_*292dup
ENST00000343932.4:c.*291_*292dup	ENSP00000342007.4:n.*291_*292dup
NM_000761.4:c.*291_*292dup	NP_000752.2:n.*291_*292dup
NM_000761.5:c.*291_*292dup MANE Select	NP_000752.2:n.*291_*292dup