Canonical Allele Identifier: CA971498259
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs2063303752

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749516_74749519del , CM000677.2:g.74749516_74749519del GRCh38
NC_000015.9:g.75041857_75041860del , CM000677.1:g.75041857_75041860del GRCh37
NC_000015.8:g.72828910_72828913del NCBI36
NG_008431.1:g.31975_31978del
NG_008431.2:g.31975_31978del
NG_061543.1:g.5672_5675del

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.-9-214_-9-211del MANE Select ENSP00000342007.4:n.-9-214_-9-211del
ENST00000343932.4:c.-9-214_-9-211del ENSP00000342007.4:n.-9-214_-9-211del
NM_000761.4:c.-9-214_-9-211del NP_000752.2:n.-9-214_-9-211del
NM_000761.5:c.-9-214_-9-211del MANE Select NP_000752.2:n.-9-214_-9-211del