Canonical Allele Identifier: CA2629509740
Gene: CYP1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74752089del , CM000677.2:g.74752089del GRCh38
NC_000015.9:g.75044430del , CM000677.1:g.75044430del GRCh37
NC_000015.8:g.72831483del NCBI36
NG_008431.1:g.34548del
NG_008431.2:g.34548del
NG_061543.1:g.8245del

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.1043-35del MANE Select ENSP00000342007.4:n.1043-35del
ENST00000343932.4:c.1043-35del ENSP00000342007.4:n.1043-35del
NM_000761.4:c.1043-35del NP_000752.2:n.1043-35del
NM_000761.5:c.1043-35del MANE Select NP_000752.2:n.1043-35del