Canonical Allele Identifier: CA2187824615
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749847A= , CM000677.2:g.74749847A= GRCh38
NC_000015.9:g.75042188A= , CM000677.1:g.75042188A= GRCh37
NC_000015.8:g.72829241A= NCBI36
NG_008431.1:g.32306A=
NG_008431.2:g.32306A=
NG_061543.1:g.6003A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.109A= MANE Select ENSP00000342007.4:p.Lys37=
ENST00000343932.4:c.109A= ENSP00000342007.4:p.Lys37=
NM_000761.4:c.109A= NP_000752.2:p.Lys37=
NM_000761.5:c.109A= MANE Select NP_000752.2:p.Lys37=