Canonical Allele Identifier: CA2629512131
Gene: CYP1A2 HGNC NCBI

Linked Data

gnomAD v4: 15-74755298-CT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755299del , CM000677.2:g.74755299del GRCh38
NC_000015.9:g.75047640del , CM000677.1:g.75047640del GRCh37
NC_000015.8:g.72834693del NCBI36
NG_008431.1:g.37758del
NG_008431.2:g.37758del
NG_061543.1:g.11455del

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*211del MANE Select ENSP00000342007.4:n.*211del
ENST00000343932.4:c.*211del ENSP00000342007.4:n.*211del
NM_000761.4:c.*211del NP_000752.2:n.*211del
NM_000761.5:c.*211del MANE Select NP_000752.2:n.*211del
Search 100 bp 5'
Search 100 bp 3'