Canonical Allele Identifier: CA2629512243
Gene: CYP1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755390_74755391dup , CM000677.2:g.74755390_74755391dup GRCh38
NC_000015.9:g.75047731_75047732dup , CM000677.1:g.75047731_75047732dup GRCh37
NC_000015.8:g.72834784_72834785dup NCBI36
NG_008431.1:g.37849_37850dup
NG_008431.2:g.37849_37850dup
NG_061543.1:g.11546_11547dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*302_*303dup MANE Select ENSP00000342007.4:n.*302_*303dup
ENST00000343932.4:c.*302_*303dup ENSP00000342007.4:n.*302_*303dup
NM_000761.4:c.*302_*303dup NP_000752.2:n.*302_*303dup
NM_000761.5:c.*302_*303dup MANE Select NP_000752.2:n.*302_*303dup