Canonical Allele Identifier: CA14148631
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs3743484

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74752059G>C , CM000677.2:g.74752059G>C GRCh38
NC_000015.9:g.75044400G>C , CM000677.1:g.75044400G>C GRCh37
NC_000015.8:g.72831453G>C NCBI36
NG_008431.1:g.34518G>C
NG_008431.2:g.34518G>C
NG_061543.1:g.8215G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.1043-65G>C MANE Select ENSP00000342007.4:p.=
ENST00000343932.4:c.1043-65G>C ENSP00000342007.4:p.=
NM_000761.4:c.1043-65G>C NP_000752.2:p.=
NM_000761.5:c.1043-65G>C MANE Select NP_000752.2:p.=