Canonical Allele Identifier: CA715672214

Gene: CYP1A2

Linked Data

• dbSNP Id: rs1378700641
• gnomAD v3: 15-74749517-C-CT
• gnomAD v4: 15-74749517-C-CT
• MyVariant Identifiers: chr15:g.75041858_75041859insT (hg19) ; chr15:g.74749517_74749518insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74749519dup , CM000677.2:g.74749519dup	GRCh38
NC_000015.9:g.75041860dup , CM000677.1:g.75041860dup	GRCh37
NC_000015.8:g.72828913dup	NCBI36
NG_008431.1:g.31978dup
NG_008431.2:g.31978dup
NG_061543.1:g.5675dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000343932.5:c.-9-211dup MANE Select	ENSP00000342007.4:n.-9-211dup
ENST00000343932.4:c.-9-211dup	ENSP00000342007.4:n.-9-211dup
NM_000761.4:c.-9-211dup	NP_000752.2:n.-9-211dup
NM_000761.5:c.-9-211dup MANE Select	NP_000752.2:n.-9-211dup