Canonical Allele Identifier: CA2629512202

Gene: CYP1A2

Linked Data

• gnomAD v4: 15-74755348-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74755349dup , CM000677.2:g.74755349dup	GRCh38
NC_000015.9:g.75047690dup , CM000677.1:g.75047690dup	GRCh37
NC_000015.8:g.72834743dup	NCBI36
NG_008431.1:g.37808dup
NG_008431.2:g.37808dup
NG_061543.1:g.11505dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343932.5:c.*261dup MANE Select	ENSP00000342007.4:n.*261dup
ENST00000343932.4:c.*261dup	ENSP00000342007.4:n.*261dup
NM_000761.4:c.*261dup	NP_000752.2:n.*261dup
NM_000761.5:c.*261dup MANE Select	NP_000752.2:n.*261dup