Canonical Allele Identifier: CA2629512221
Gene: CYP1A2 HGNC NCBI

Linked Data

gnomAD v4: 15-74755362-CAAACA-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755365_74755369del , CM000677.2:g.74755365_74755369del GRCh38
NC_000015.9:g.75047706_75047710del , CM000677.1:g.75047706_75047710del GRCh37
NC_000015.8:g.72834759_72834763del NCBI36
NG_008431.1:g.37824_37828del
NG_008431.2:g.37824_37828del
NG_061543.1:g.11521_11525del

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*277_*281del MANE Select ENSP00000342007.4:n.*277_*281del
ENST00000343932.4:c.*277_*281del ENSP00000342007.4:n.*277_*281del
NM_000761.4:c.*277_*281del NP_000752.2:n.*277_*281del
NM_000761.5:c.*277_*281del MANE Select NP_000752.2:n.*277_*281del
Search 100 bp 5'
Search 100 bp 3'