Canonical Allele Identifier: CA393177981
Gene: CYP1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74750015A>G , CM000677.2:g.74750015A>G GRCh38
NC_000015.9:g.75042356A>G , CM000677.1:g.75042356A>G GRCh37
NC_000015.8:g.72829409A>G NCBI36
NG_008431.1:g.32474A>G
NG_008431.2:g.32474A>G
NG_061543.1:g.6171A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.277A>G MANE Select ENSP00000342007.4:p.Thr93Ala
ENST00000343932.4:c.277A>G ENSP00000342007.4:p.Thr93Ala
NM_000761.4:c.277A>G NP_000752.2:p.Thr93Ala
NM_000761.5:c.277A>G MANE Select NP_000752.2:p.Thr93Ala