Canonical Allele Identifier: CA971501128

Gene: CYP1A2

Linked Data

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

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74755377_74755380dup , CM000677.2:g.74755377_74755380dup	GRCh38
NC_000015.9:g.75047718_75047721dup , CM000677.1:g.75047718_75047721dup	GRCh37
NC_000015.8:g.72834771_72834774dup	NCBI36
NG_008431.1:g.37836_37839dup
NG_008431.2:g.37836_37839dup
NG_061543.1:g.11533_11536dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343932.5:c.*289_*292dup MANE Select	ENSP00000342007.4:n.*289_*292dup
ENST00000343932.4:c.*289_*292dup	ENSP00000342007.4:n.*289_*292dup
NM_000761.4:c.*289_*292dup	NP_000752.2:n.*289_*292dup
NM_000761.5:c.*289_*292dup MANE Select	NP_000752.2:n.*289_*292dup