Canonical Allele Identifier: CA2187826949
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74754614A= , CM000677.2:g.74754614A= GRCh38
NC_000015.9:g.75046955A= , CM000677.1:g.75046955A= GRCh37
NC_000015.8:g.72834008A= NCBI36
NG_008431.1:g.37073A=
NG_008431.2:g.37073A=
NG_061543.1:g.10770A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.1254-177A= MANE Select ENSP00000342007.4:n.1254-177A=
ENST00000343932.4:c.1254-177A= ENSP00000342007.4:n.1254-177A=
NM_000761.4:c.1254-177A= NP_000752.2:n.1254-177A=
NM_000761.5:c.1254-177A= MANE Select NP_000752.2:n.1254-177A=