Canonical Allele Identifier: CA2187827275

Gene: CYP1A2

Linked Data

• dbSNP Id: rs2063333198

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74755308_74755309insG , CM000677.2:g.74755308_74755309insG	GRCh38
NC_000015.9:g.75047649_75047650insG , CM000677.1:g.75047649_75047650insG	GRCh37
NC_000015.8:g.72834702_72834703insG	NCBI36
NG_008431.1:g.37767_37768insG
NG_008431.2:g.37767_37768insG
NG_061543.1:g.11464_11465insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343932.5:c.*220_*221insG MANE Select	ENSP00000342007.4:n.*220_*221insG
ENST00000343932.4:c.*220_*221insG	ENSP00000342007.4:n.*220_*221insG
NM_000761.4:c.*220_*221insG	NP_000752.2:n.*220_*221insG
NM_000761.5:c.*220_*221insG MANE Select	NP_000752.2:n.*220_*221insG