Canonical Allele Identifier: CA2187824765
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs2063307411
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74750159del , CM000677.2:g.74750159del GRCh38
NC_000015.9:g.75042500del , CM000677.1:g.75042500del GRCh37
NC_000015.8:g.72829553del NCBI36
NG_008431.1:g.32618del
NG_008431.2:g.32618del
NG_061543.1:g.6315del

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.421del MANE Select ENSP00000342007.4:p.Gln141ArgfsTer25
ENST00000343932.4:c.421del ENSP00000342007.4:p.Gln141ArgfsTer25
NM_000761.4:c.421del NP_000752.2:p.Gln141ArgfsTer25
NM_000761.5:c.421del MANE Select NP_000752.2:p.Gln141ArgfsTer25
Search 100 bp 5'
Search 100 bp 3'