Canonical Allele Identifier: CA2187824466
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749478T= , CM000677.2:g.74749478T= GRCh38
NC_000015.9:g.75041819T= , CM000677.1:g.75041819T= GRCh37
NC_000015.8:g.72828872T= NCBI36
NG_008431.1:g.31937T=
NG_008431.2:g.31937T=
NG_061543.1:g.5634T=

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.-9-252T= MANE Select ENSP00000342007.4:n.-9-252T=
ENST00000343932.4:c.-9-252T= ENSP00000342007.4:n.-9-252T=
NM_000761.4:c.-9-252T= NP_000752.2:n.-9-252T=
NM_000761.5:c.-9-252T= MANE Select NP_000752.2:n.-9-252T=