Canonical Allele Identifier: CA2629512148
Gene: CYP1A2 HGNC NCBI

Linked Data

gnomAD v4: 15-74755311-A-AG
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755311_74755312insG , CM000677.2:g.74755311_74755312insG GRCh38
NC_000015.9:g.75047652_75047653insG , CM000677.1:g.75047652_75047653insG GRCh37
NC_000015.8:g.72834705_72834706insG NCBI36
NG_008431.1:g.37770_37771insG
NG_008431.2:g.37770_37771insG
NG_061543.1:g.11467_11468insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*223_*224insG MANE Select ENSP00000342007.4:n.*223_*224insG
ENST00000343932.4:c.*223_*224insG ENSP00000342007.4:n.*223_*224insG
NM_000761.4:c.*223_*224insG NP_000752.2:n.*223_*224insG
NM_000761.5:c.*223_*224insG MANE Select NP_000752.2:n.*223_*224insG
Search 100 bp 5'
Search 100 bp 3'