Canonical Allele Identifier: CA2187824519
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs1875711135

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749614del , CM000677.2:g.74749614del GRCh38
NC_000015.9:g.75041955del , CM000677.1:g.75041955del GRCh37
NC_000015.8:g.72829008del NCBI36
NG_008431.1:g.32073del
NG_008431.2:g.32073del
NG_061543.1:g.5770del

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.-9-116del MANE Select ENSP00000342007.4:p.=
ENST00000343932.4:c.-9-116del ENSP00000342007.4:p.=
NM_000761.4:c.-9-116del NP_000752.2:p.=
NM_000761.5:c.-9-116del MANE Select NP_000752.2:p.=