Canonical Allele Identifier: CA2187827196
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755098C= , CM000677.2:g.74755098C= GRCh38
NC_000015.9:g.75047439C= , CM000677.1:g.75047439C= GRCh37
NC_000015.8:g.72834492C= NCBI36
NG_008431.1:g.37557C=
NG_008431.2:g.37557C=
NG_061543.1:g.11254C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*10C= MANE Select ENSP00000342007.4:n.*10C=
ENST00000343932.4:c.*10C= ENSP00000342007.4:n.*10C=
NM_000761.4:c.*10C= NP_000752.2:n.*10C=
NM_000761.5:c.*10C= MANE Select NP_000752.2:n.*10C=