Canonical Allele Identifier: CA2596105645
Gene: CYP1A2 HGNC NCBI

Linked Data

gnomAD v3: 15-74755371-A-AC
gnomAD v4: 15-74755371-A-AC
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755371_74755372insC , CM000677.2:g.74755371_74755372insC GRCh38
NC_000015.9:g.75047712_75047713insC , CM000677.1:g.75047712_75047713insC GRCh37
NC_000015.8:g.72834765_72834766insC NCBI36
NG_008431.1:g.37830_37831insC
NG_008431.2:g.37830_37831insC
NG_061543.1:g.11527_11528insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*283_*284insC MANE Select ENSP00000342007.4:n.*283_*284insC
ENST00000343932.4:c.*283_*284insC ENSP00000342007.4:n.*283_*284insC
NM_000761.4:c.*283_*284insC NP_000752.2:n.*283_*284insC
NM_000761.5:c.*283_*284insC MANE Select NP_000752.2:n.*283_*284insC
Search 100 bp 5'
Search 100 bp 3'