Canonical Allele Identifier: CA2187827209
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755124G= , CM000677.2:g.74755124G= GRCh38
NC_000015.9:g.75047465G= , CM000677.1:g.75047465G= GRCh37
NC_000015.8:g.72834518G= NCBI36
NG_008431.1:g.37583G=
NG_008431.2:g.37583G=
NG_061543.1:g.11280G=

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.*36G= MANE Select ENSP00000342007.4:n.*36G=
ENST00000343932.4:c.*36G= ENSP00000342007.4:n.*36G=
NM_000761.4:c.*36G= NP_000752.2:n.*36G=
NM_000761.5:c.*36G= MANE Select NP_000752.2:n.*36G=