Canonical Allele Identifier: CA2187826991
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74754704G= , CM000677.2:g.74754704G= GRCh38
NC_000015.9:g.75047045G= , CM000677.1:g.75047045G= GRCh37
NC_000015.8:g.72834098G= NCBI36
NG_008431.1:g.37163G=
NG_008431.2:g.37163G=
NG_061543.1:g.10860G=

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.1254-87G= MANE Select ENSP00000342007.4:n.1254-87G=
ENST00000343932.4:c.1254-87G= ENSP00000342007.4:n.1254-87G=
NM_000761.4:c.1254-87G= NP_000752.2:n.1254-87G=
NM_000761.5:c.1254-87G= MANE Select NP_000752.2:n.1254-87G=