Canonical Allele Identifier: CA2629512057
Gene: CYP1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755254del , CM000677.2:g.74755254del GRCh38
NC_000015.9:g.75047595del , CM000677.1:g.75047595del GRCh37
NC_000015.8:g.72834648del NCBI36
NG_008431.1:g.37713del
NG_008431.2:g.37713del
NG_061543.1:g.11410del

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*166del MANE Select ENSP00000342007.4:n.*166del
ENST00000343932.4:c.*166del ENSP00000342007.4:n.*166del
NM_000761.4:c.*166del NP_000752.2:n.*166del
NM_000761.5:c.*166del MANE Select NP_000752.2:n.*166del