Canonical Allele Identifier: CA2629503351
Gene: CYP1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74748880A>G , CM000677.2:g.74748880A>G GRCh38
NC_000015.9:g.75041221A>G , CM000677.1:g.75041221A>G GRCh37
NC_000015.8:g.72828274A>G NCBI36
NG_008431.1:g.31339A>G
NG_008431.2:g.31339A>G
NG_061543.1:g.5036A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.-27A>G MANE Select ENSP00000342007.4:n.-27A>G
ENST00000343932.4:c.-27A>G ENSP00000342007.4:n.-27A>G
NM_000761.4:c.-27A>G NP_000752.2:n.-27A>G
NM_000761.5:c.-27A>G MANE Select NP_000752.2:n.-27A>G