Canonical Allele Identifier: CA393177197
Gene: CYP1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749863C>A , CM000677.2:g.74749863C>A GRCh38
NC_000015.9:g.75042204C>A , CM000677.1:g.75042204C>A GRCh37
NC_000015.8:g.72829257C>A NCBI36
NG_008431.1:g.32322C>A
NG_008431.2:g.32322C>A
NG_061543.1:g.6019C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.125C>A MANE Select ENSP00000342007.4:p.Pro42Gln
ENST00000343932.4:c.125C>A ENSP00000342007.4:p.Pro42Gln
NM_000761.4:c.125C>A NP_000752.2:p.Pro42Gln
NM_000761.5:c.125C>A MANE Select NP_000752.2:p.Pro42Gln