Canonical Allele Identifier: CA2187827337

Gene: CYP1A2

Linked Data

• dbSNP Id: rs2063333799
• gnomAD v4: 15-74755372-A-AC

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74755372_74755373insC , CM000677.2:g.74755372_74755373insC	GRCh38
NC_000015.9:g.75047713_75047714insC , CM000677.1:g.75047713_75047714insC	GRCh37
NC_000015.8:g.72834766_72834767insC	NCBI36
NG_008431.1:g.37831_37832insC
NG_008431.2:g.37831_37832insC
NG_061543.1:g.11528_11529insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343932.5:c.*284_*285insC MANE Select	ENSP00000342007.4:n.*284_*285insC
ENST00000343932.4:c.*284_*285insC	ENSP00000342007.4:n.*284_*285insC
NM_000761.4:c.*284_*285insC	NP_000752.2:n.*284_*285insC
NM_000761.5:c.*284_*285insC MANE Select	NP_000752.2:n.*284_*285insC