Canonical Allele Identifier: CA2629512133
Gene: CYP1A2 HGNC NCBI

Linked Data

gnomAD v4: 15-74755299-T-TA
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755300dup , CM000677.2:g.74755300dup GRCh38
NC_000015.9:g.75047641dup , CM000677.1:g.75047641dup GRCh37
NC_000015.8:g.72834694dup NCBI36
NG_008431.1:g.37759dup
NG_008431.2:g.37759dup
NG_061543.1:g.11456dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*212dup MANE Select ENSP00000342007.4:n.*212dup
ENST00000343932.4:c.*212dup ENSP00000342007.4:n.*212dup
NM_000761.4:c.*212dup NP_000752.2:n.*212dup
NM_000761.5:c.*212dup MANE Select NP_000752.2:n.*212dup
Search 100 bp 5'
Search 100 bp 3'