Canonical Allele Identifier: CA2187824194
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs1877203592

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74748875A>G , CM000677.2:g.74748875A>G GRCh38
NC_000015.9:g.75041216A>G , CM000677.1:g.75041216A>G GRCh37
NC_000015.8:g.72828269A>G NCBI36
NG_008431.1:g.31334A>G
NG_008431.2:g.31334A>G
NG_061543.1:g.5031A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.-32A>G MANE Select ENSP00000342007.4:n.-32A>G
ENST00000343932.4:c.-32A>G ENSP00000342007.4:n.-32A>G
NM_000761.4:c.-32A>G NP_000752.2:n.-32A>G
NM_000761.5:c.-32A>G MANE Select NP_000752.2:n.-32A>G