Canonical Allele Identifier: CA2187826978
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74754680C= , CM000677.2:g.74754680C= GRCh38
NC_000015.9:g.75047021C= , CM000677.1:g.75047021C= GRCh37
NC_000015.8:g.72834074C= NCBI36
NG_008431.1:g.37139C=
NG_008431.2:g.37139C=
NG_061543.1:g.10836C=

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.1254-111C= MANE Select ENSP00000342007.4:n.1254-111C=
ENST00000343932.4:c.1254-111C= ENSP00000342007.4:n.1254-111C=
NM_000761.4:c.1254-111C= NP_000752.2:n.1254-111C=
NM_000761.5:c.1254-111C= MANE Select NP_000752.2:n.1254-111C=