Canonical Allele Identifier: CA2629509239
Gene: CYP1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74751855del , CM000677.2:g.74751855del GRCh38
NC_000015.9:g.75044196del , CM000677.1:g.75044196del GRCh37
NC_000015.8:g.72831249del NCBI36
NG_008431.1:g.34314del
NG_008431.2:g.34314del
NG_061543.1:g.8011del

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.1042+1del
ENST00000343932.4:c.1042+1del
NM_000761.4:c.1042+1del
NM_000761.5:c.1042+1del