Canonical Allele Identifier: CA272815221
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs190776263

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74751999G>T , CM000677.2:g.74751999G>T GRCh38
NC_000015.9:g.75044340G>T , CM000677.1:g.75044340G>T GRCh37
NC_000015.8:g.72831393G>T NCBI36
NG_008431.1:g.34458G>T
NG_008431.2:g.34458G>T
NG_061543.1:g.8155G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.1043-125G>T MANE Select ENSP00000342007.4:n.1043-125G>T
ENST00000343932.4:c.1043-125G>T ENSP00000342007.4:n.1043-125G>T
NM_000761.4:c.1043-125G>T NP_000752.2:n.1043-125G>T
NM_000761.5:c.1043-125G>T MANE Select NP_000752.2:n.1043-125G>T