Canonical Allele Identifier: CA2629512222
Gene: CYP1A2 HGNC NCBI

Linked Data

gnomAD v4: 15-74755363-AAAC-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755366_74755368del , CM000677.2:g.74755366_74755368del GRCh38
NC_000015.9:g.75047707_75047709del , CM000677.1:g.75047707_75047709del GRCh37
NC_000015.8:g.72834760_72834762del NCBI36
NG_008431.1:g.37825_37827del
NG_008431.2:g.37825_37827del
NG_061543.1:g.11522_11524del

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*278_*280del MANE Select ENSP00000342007.4:n.*278_*280del
ENST00000343932.4:c.*278_*280del ENSP00000342007.4:n.*278_*280del
NM_000761.4:c.*278_*280del NP_000752.2:n.*278_*280del
NM_000761.5:c.*278_*280del MANE Select NP_000752.2:n.*278_*280del
Search 100 bp 5'
Search 100 bp 3'