Canonical Allele Identifier: CA619412760
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs1204941667

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74752079A>G , CM000677.2:g.74752079A>G GRCh38
NC_000015.9:g.75044420A>G , CM000677.1:g.75044420A>G GRCh37
NC_000015.8:g.72831473A>G NCBI36
NG_008431.1:g.34538A>G
NG_008431.2:g.34538A>G
NG_061543.1:g.8235A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.1043-45A>G MANE Select ENSP00000342007.4:n.1043-45A>G
ENST00000343932.4:c.1043-45A>G ENSP00000342007.4:n.1043-45A>G
NM_000761.4:c.1043-45A>G NP_000752.2:n.1043-45A>G
NM_000761.5:c.1043-45A>G MANE Select NP_000752.2:n.1043-45A>G