Canonical Allele Identifier: CA2629512218
Gene: CYP1A2 HGNC NCBI

Linked Data

gnomAD v4: 15-74755360-AACAAAC-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755362_74755367del , CM000677.2:g.74755362_74755367del GRCh38
NC_000015.9:g.75047703_75047708del , CM000677.1:g.75047703_75047708del GRCh37
NC_000015.8:g.72834756_72834761del NCBI36
NG_008431.1:g.37821_37826del
NG_008431.2:g.37821_37826del
NG_061543.1:g.11518_11523del

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*274_*279del MANE Select ENSP00000342007.4:n.*274_*279del
ENST00000343932.4:c.*274_*279del ENSP00000342007.4:n.*274_*279del
NM_000761.4:c.*274_*279del NP_000752.2:n.*274_*279del
NM_000761.5:c.*274_*279del MANE Select NP_000752.2:n.*274_*279del
Search 100 bp 5'
Search 100 bp 3'