Canonical Allele Identifier: CA2187826936
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74754583A= , CM000677.2:g.74754583A= GRCh38
NC_000015.9:g.75046924A= , CM000677.1:g.75046924A= GRCh37
NC_000015.8:g.72833977A= NCBI36
NG_008431.1:g.37042A=
NG_008431.2:g.37042A=
NG_061543.1:g.10739A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.1254-208A= MANE Select ENSP00000342007.4:n.1254-208A=
ENST00000343932.4:c.1254-208A= ENSP00000342007.4:n.1254-208A=
NM_000761.4:c.1254-208A= NP_000752.2:n.1254-208A=
NM_000761.5:c.1254-208A= MANE Select NP_000752.2:n.1254-208A=