Canonical Allele Identifier: CA971501016
Gene: CYP1A2 HGNC NCBI

Linked Data

gnomAD v3: 15-74755294-GTCTCT-G
gnomAD v4: 15-74755294-GTCTCT-G
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755295_74755299del , CM000677.2:g.74755295_74755299del GRCh38
NC_000015.9:g.75047636_75047640del , CM000677.1:g.75047636_75047640del GRCh37
NC_000015.8:g.72834689_72834693del NCBI36
NG_008431.1:g.37754_37758del
NG_008431.2:g.37754_37758del
NG_061543.1:g.11451_11455del

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*207_*211del MANE Select ENSP00000342007.4:n.*207_*211del
ENST00000343932.4:c.*207_*211del ENSP00000342007.4:n.*207_*211del
NM_000761.4:c.*207_*211del NP_000752.2:n.*207_*211del
NM_000761.5:c.*207_*211del MANE Select NP_000752.2:n.*207_*211del
Search 100 bp 5'
Search 100 bp 3'