Canonical Allele Identifier: CA2629504420
Gene: CYP1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749692del , CM000677.2:g.74749692del GRCh38
NC_000015.9:g.75042033del , CM000677.1:g.75042033del GRCh37
NC_000015.8:g.72829086del NCBI36
NG_008431.1:g.32151del
NG_008431.2:g.32151del
NG_061543.1:g.5848del

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.-9-38del MANE Select ENSP00000342007.4:n.-9-38del
ENST00000343932.4:c.-9-38del ENSP00000342007.4:n.-9-38del
NM_000761.4:c.-9-38del NP_000752.2:n.-9-38del
NM_000761.5:c.-9-38del MANE Select NP_000752.2:n.-9-38del