Canonical Allele Identifier: CA2629511986
Gene: CYP1A2 HGNC NCBI

Linked Data

gnomAD v4: 15-74755173-TA-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755179del , CM000677.2:g.74755179del GRCh38
NC_000015.9:g.75047520del , CM000677.1:g.75047520del GRCh37
NC_000015.8:g.72834573del NCBI36
NG_008431.1:g.37638del
NG_008431.2:g.37638del
NG_061543.1:g.11335del

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*91del MANE Select ENSP00000342007.4:n.*91del
ENST00000343932.4:c.*91del ENSP00000342007.4:n.*91del
NM_000761.4:c.*91del NP_000752.2:n.*91del
NM_000761.5:c.*91del MANE Select NP_000752.2:n.*91del
Search 100 bp 5'
Search 100 bp 3'