Canonical Allele Identifier: CA619123147
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs1248862345

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755365del , CM000677.2:g.74755365del GRCh38
NC_000015.9:g.75047706del , CM000677.1:g.75047706del GRCh37
NC_000015.8:g.72834759del NCBI36
NG_008431.1:g.37824del
NG_008431.2:g.37824del
NG_061543.1:g.11521del

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*277del MANE Select ENSP00000342007.4:n.*277del
ENST00000343932.4:c.*277del ENSP00000342007.4:n.*277del
NM_000761.4:c.*277del NP_000752.2:n.*277del
NM_000761.5:c.*277del MANE Select NP_000752.2:n.*277del