Canonical Allele Identifier: CA272820279
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs545591270

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749621G>A , CM000677.2:g.74749621G>A GRCh38
NC_000015.9:g.75041962G>A , CM000677.1:g.75041962G>A GRCh37
NC_000015.8:g.72829015G>A NCBI36
NG_008431.1:g.32080G>A
NG_008431.2:g.32080G>A
NG_061543.1:g.5777G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.-9-109G>A MANE Select ENSP00000342007.4:p.=
ENST00000343932.4:c.-9-109G>A ENSP00000342007.4:p.=
NM_000761.4:c.-9-109G>A NP_000752.2:p.=
NM_000761.5:c.-9-109G>A MANE Select NP_000752.2:p.=