Canonical Allele Identifier: CA2629503251
Gene: CYP1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74748844A>G , CM000677.2:g.74748844A>G GRCh38
NC_000015.9:g.75041185A>G , CM000677.1:g.75041185A>G GRCh37
NC_000015.8:g.72828238A>G NCBI36
NG_008431.1:g.31303A>G
NG_008431.2:g.31303A>G
NG_061543.1:g.5000A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.4:c.-63A>G ENSP00000342007.4:n.-63A>G
NM_000761.4:c.-63A>G NP_000752.2:n.-63A>G