Canonical Allele Identifier: CA2629511985
Gene: CYP1A2 HGNC NCBI

Linked Data

gnomAD v4: 15-74755173-T-TA
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755179dup , CM000677.2:g.74755179dup GRCh38
NC_000015.9:g.75047520dup , CM000677.1:g.75047520dup GRCh37
NC_000015.8:g.72834573dup NCBI36
NG_008431.1:g.37638dup
NG_008431.2:g.37638dup
NG_061543.1:g.11335dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*91dup MANE Select ENSP00000342007.4:n.*91dup
ENST00000343932.4:c.*91dup ENSP00000342007.4:n.*91dup
NM_000761.4:c.*91dup NP_000752.2:n.*91dup
NM_000761.5:c.*91dup MANE Select NP_000752.2:n.*91dup
Search 100 bp 5'
Search 100 bp 3'