Canonical Allele Identifier: CA619123036
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs1178960248

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74754801del , CM000677.2:g.74754801del GRCh38
NC_000015.9:g.75047142del , CM000677.1:g.75047142del GRCh37
NC_000015.8:g.72834195del NCBI36
NG_008431.1:g.37260del
NG_008431.2:g.37260del
NG_061543.1:g.10957del

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.1264del MANE Select ENSP00000342007.4:p.Glu422ArgfsTer23
ENST00000343932.4:c.1264del ENSP00000342007.4:p.Glu422ArgfsTer23
NM_000761.4:c.1264del NP_000752.2:p.Glu422ArgfsTer23
NM_000761.5:c.1264del MANE Select NP_000752.2:p.Glu422ArgfsTer23