Canonical Allele Identifier: CA715672246
Gene: CYP1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749585A>G , CM000677.2:g.74749585A>G GRCh38
NC_000015.9:g.75041926A>G , CM000677.1:g.75041926A>G GRCh37
NC_000015.8:g.72828979A>G NCBI36
NG_008431.1:g.32044A>G
NG_008431.2:g.32044A>G
NG_061543.1:g.5741A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.-9-145A>G MANE Select ENSP00000342007.4:p.=
ENST00000343932.4:c.-9-145A>G ENSP00000342007.4:p.=
NM_000761.4:c.-9-145A>G NP_000752.2:p.=
NM_000761.5:c.-9-145A>G MANE Select NP_000752.2:p.=