Canonical Allele Identifier: CA2629512139
Gene: CYP1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755309_74755311dup , CM000677.2:g.74755309_74755311dup GRCh38
NC_000015.9:g.75047650_75047652dup , CM000677.1:g.75047650_75047652dup GRCh37
NC_000015.8:g.72834703_72834705dup NCBI36
NG_008431.1:g.37768_37770dup
NG_008431.2:g.37768_37770dup
NG_061543.1:g.11465_11467dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*221_*223dup MANE Select ENSP00000342007.4:n.*221_*223dup
ENST00000343932.4:c.*221_*223dup ENSP00000342007.4:n.*221_*223dup
NM_000761.4:c.*221_*223dup NP_000752.2:n.*221_*223dup
NM_000761.5:c.*221_*223dup MANE Select NP_000752.2:n.*221_*223dup