Canonical Allele Identifier: CA715672258
Gene: CYP1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749627C>A , CM000677.2:g.74749627C>A GRCh38
NC_000015.9:g.75041968C>A , CM000677.1:g.75041968C>A GRCh37
NC_000015.8:g.72829021C>A NCBI36
NG_008431.1:g.32086C>A
NG_008431.2:g.32086C>A
NG_061543.1:g.5783C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.-9-103C>A MANE Select ENSP00000342007.4:p.=
ENST00000343932.4:c.-9-103C>A ENSP00000342007.4:p.=
NM_000761.4:c.-9-103C>A NP_000752.2:p.=
NM_000761.5:c.-9-103C>A MANE Select NP_000752.2:p.=