Canonical Allele Identifier: CA2506762122
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749492G>C , CM000677.2:g.74749492G>C GRCh38
NC_000015.9:g.75041833G>C , CM000677.1:g.75041833G>C GRCh37
NC_000015.8:g.72828886G>C NCBI36
NG_008431.1:g.31951G>C
NG_008431.2:g.31951G>C
NG_061543.1:g.5648G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.-9-238G>C MANE Select ENSP00000342007.4:n.-9-238G>C
ENST00000343932.4:c.-9-238G>C ENSP00000342007.4:n.-9-238G>C
NM_000761.4:c.-9-238G>C NP_000752.2:n.-9-238G>C
NM_000761.5:c.-9-238G>C MANE Select NP_000752.2:n.-9-238G>C