Canonical Allele Identifier: CA14135597
Gene: CYP1A2 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 511079
ClinVar RCV Id: RCV000607978
dbSNP Id: rs762551

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749576C>A , CM000677.2:g.74749576C>A GRCh38
NC_000015.9:g.75041917C>A , CM000677.1:g.75041917C>A GRCh37
NC_000015.8:g.72828970C>A NCBI36
NG_008431.1:g.32035C>A
NG_008431.2:g.32035C>A
NG_061543.1:g.5732C>A

Transcript Alleles

HGVS Amino-acid change
NM_000761.4:c.-9-154C>A VV NP_000752.2:p.=
NM_000761.5:c.-9-154C>A VV NP_000752.2:p.=
ENST00000343932.4:c.-9-154C>A ENSP00000342007.4:p.=