Canonical Allele Identifier: CA2187824606
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749829T= , CM000677.2:g.74749829T= GRCh38
NC_000015.9:g.75042170T= , CM000677.1:g.75042170T= GRCh37
NC_000015.8:g.72829223T= NCBI36
NG_008431.1:g.32288T=
NG_008431.2:g.32288T=
NG_061543.1:g.5985T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.91T= MANE Select ENSP00000342007.4:p.Leu31=
ENST00000343932.4:c.91T= ENSP00000342007.4:p.Leu31=
NM_000761.4:c.91T= NP_000752.2:p.Leu31=
NM_000761.5:c.91T= MANE Select NP_000752.2:p.Leu31=