Canonical Allele Identifier: CA7659960
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs370133366

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74752074G>A , CM000677.2:g.74752074G>A GRCh38
NC_000015.9:g.75044415G>A , CM000677.1:g.75044415G>A GRCh37
NC_000015.8:g.72831468G>A NCBI36
NG_008431.1:g.34533G>A
NG_008431.2:g.34533G>A
NG_061543.1:g.8230G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.1043-50G>A MANE Select ENSP00000342007.4:n.1043-50G>A
ENST00000343932.4:c.1043-50G>A ENSP00000342007.4:n.1043-50G>A
NM_000761.4:c.1043-50G>A NP_000752.2:n.1043-50G>A
NM_000761.5:c.1043-50G>A MANE Select NP_000752.2:n.1043-50G>A