Canonical Allele Identifier: CA2629512227
Gene: CYP1A2 HGNC NCBI

Linked Data

gnomAD v4: 15-74755366-C-CAA
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755368_74755369dup , CM000677.2:g.74755368_74755369dup GRCh38
NC_000015.9:g.75047709_75047710dup , CM000677.1:g.75047709_75047710dup GRCh37
NC_000015.8:g.72834762_72834763dup NCBI36
NG_008431.1:g.37827_37828dup
NG_008431.2:g.37827_37828dup
NG_061543.1:g.11524_11525dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*280_*281dup MANE Select ENSP00000342007.4:n.*280_*281dup
ENST00000343932.4:c.*280_*281dup ENSP00000342007.4:n.*280_*281dup
NM_000761.4:c.*280_*281dup NP_000752.2:n.*280_*281dup
NM_000761.5:c.*280_*281dup MANE Select NP_000752.2:n.*280_*281dup
Search 100 bp 5'
Search 100 bp 3'