Canonical Allele Identifier: CA715672192
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs1356335329

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749450_74749451insT , CM000677.2:g.74749450_74749451insT GRCh38
NC_000015.9:g.75041791_75041792insT , CM000677.1:g.75041791_75041792insT GRCh37
NC_000015.8:g.72828844_72828845insT NCBI36
NG_008431.1:g.31909_31910insT
NG_008431.2:g.31909_31910insT
NG_061543.1:g.5606_5607insT

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.-9-280_-9-279insT MANE Select ENSP00000342007.4:n.-9-280_-9-279insT
ENST00000343932.4:c.-9-280_-9-279insT ENSP00000342007.4:n.-9-280_-9-279insT
NM_000761.4:c.-9-280_-9-279insT NP_000752.2:n.-9-280_-9-279insT
NM_000761.5:c.-9-280_-9-279insT MANE Select NP_000752.2:n.-9-280_-9-279insT