Canonical Allele Identifier: CA2575790179
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749710C>T , CM000677.2:g.74749710C>T GRCh38
NC_000015.9:g.75042051C>T , CM000677.1:g.75042051C>T GRCh37
NC_000015.8:g.72829104C>T NCBI36
NG_008431.1:g.32169C>T
NG_008431.2:g.32169C>T
NG_061543.1:g.5866C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.-9-20C>T MANE Select ENSP00000342007.4:n.-9-20C>T
ENST00000343932.4:c.-9-20C>T ENSP00000342007.4:n.-9-20C>T
NM_000761.4:c.-9-20C>T NP_000752.2:n.-9-20C>T
NM_000761.5:c.-9-20C>T MANE Select NP_000752.2:n.-9-20C>T