Canonical Allele Identifier: CA619121380
Gene: CYP1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749638C>T , CM000677.2:g.74749638C>T GRCh38
NC_000015.9:g.75041979C>T , CM000677.1:g.75041979C>T GRCh37
NC_000015.8:g.72829032C>T NCBI36
NG_008431.1:g.32097C>T
NG_008431.2:g.32097C>T
NG_061543.1:g.5794C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.-9-92C>T MANE Select ENSP00000342007.4:p.=
ENST00000343932.4:c.-9-92C>T ENSP00000342007.4:p.=
NM_000761.4:c.-9-92C>T NP_000752.2:p.=
NM_000761.5:c.-9-92C>T MANE Select NP_000752.2:p.=