Canonical Allele Identifier: CA715672108
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs1161826145

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74748885C>G , CM000677.2:g.74748885C>G GRCh38
NC_000015.9:g.75041226C>G , CM000677.1:g.75041226C>G GRCh37
NC_000015.8:g.72828279C>G NCBI36
NG_008431.1:g.31344C>G
NG_008431.2:g.31344C>G
NG_061543.1:g.5041C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.-22C>G MANE Select ENSP00000342007.4:n.-22C>G
ENST00000343932.4:c.-22C>G ENSP00000342007.4:n.-22C>G
NM_000761.4:c.-22C>G NP_000752.2:n.-22C>G
NM_000761.5:c.-22C>G MANE Select NP_000752.2:n.-22C>G