Canonical Allele Identifier: CA971501065
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs2063333374
gnomAD v3: 15-74755348-CT-C
gnomAD v4: 15-74755348-CT-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755349del , CM000677.2:g.74755349del GRCh38
NC_000015.9:g.75047690del , CM000677.1:g.75047690del GRCh37
NC_000015.8:g.72834743del NCBI36
NG_008431.1:g.37808del
NG_008431.2:g.37808del
NG_061543.1:g.11505del

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*261del MANE Select ENSP00000342007.4:n.*261del
ENST00000343932.4:c.*261del ENSP00000342007.4:n.*261del
NM_000761.4:c.*261del NP_000752.2:n.*261del
NM_000761.5:c.*261del MANE Select NP_000752.2:n.*261del
Search 100 bp 5'
Search 100 bp 3'