Canonical Allele Identifier: CA2629512216
Gene: CYP1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755370_74755373dup , CM000677.2:g.74755370_74755373dup GRCh38
NC_000015.9:g.75047711_75047714dup , CM000677.1:g.75047711_75047714dup GRCh37
NC_000015.8:g.72834764_72834767dup NCBI36
NG_008431.1:g.37829_37832dup
NG_008431.2:g.37829_37832dup
NG_061543.1:g.11526_11529dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*282_*285dup MANE Select ENSP00000342007.4:n.*282_*285dup
ENST00000343932.4:c.*282_*285dup ENSP00000342007.4:n.*282_*285dup
NM_000761.4:c.*282_*285dup NP_000752.2:n.*282_*285dup
NM_000761.5:c.*282_*285dup MANE Select NP_000752.2:n.*282_*285dup