Canonical Allele Identifier: CA272815657
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs55889066

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74753234G>A , CM000677.2:g.74753234G>A GRCh38
NC_000015.9:g.75045575G>A , CM000677.1:g.75045575G>A GRCh37
NC_000015.8:g.72832628G>A NCBI36
NG_008431.1:g.35693G>A
NG_008431.2:g.35693G>A
NG_061543.1:g.9390G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.1217G>A MANE Select ENSP00000342007.4:p.Cys406Tyr
ENST00000343932.4:c.1217G>A ENSP00000342007.4:p.Cys406Tyr
NM_000761.4:c.1217G>A NP_000752.2:p.Cys406Tyr
NM_000761.5:c.1217G>A MANE Select NP_000752.2:p.Cys406Tyr