Canonical Allele Identifier: CA491489315
Gene: CYP1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749864A>G , CM000677.2:g.74749864A>G GRCh38
NC_000015.9:g.75042205A>G , CM000677.1:g.75042205A>G GRCh37
NC_000015.8:g.72829258A>G NCBI36
NG_008431.1:g.32323A>G
NG_008431.2:g.32323A>G
NG_061543.1:g.6020A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.126A>G MANE Select ENSP00000342007.4:p.Pro42=
ENST00000343932.4:c.126A>G ENSP00000342007.4:p.Pro42=
NM_000761.4:c.126A>G NP_000752.2:p.Pro42=
NM_000761.5:c.126A>G MANE Select NP_000752.2:p.Pro42=