Canonical Allele Identifier: CA393176694
Gene: CYP1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749764T>G , CM000677.2:g.74749764T>G GRCh38
NC_000015.9:g.75042105T>G , CM000677.1:g.75042105T>G GRCh37
NC_000015.8:g.72829158T>G NCBI36
NG_008431.1:g.32223T>G
NG_008431.2:g.32223T>G
NG_061543.1:g.5920T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.26T>G MANE Select ENSP00000342007.4:p.Phe9Cys
ENST00000343932.4:c.26T>G ENSP00000342007.4:p.Phe9Cys
NM_000761.4:c.26T>G NP_000752.2:p.Phe9Cys
NM_000761.5:c.26T>G MANE Select NP_000752.2:p.Phe9Cys