Canonical Allele Identifier: CA7660067
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs777641092

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74754830G>C , CM000677.2:g.74754830G>C GRCh38
NC_000015.9:g.75047171G>C , CM000677.1:g.75047171G>C GRCh37
NC_000015.8:g.72834224G>C NCBI36
NG_008431.1:g.37289G>C
NG_008431.2:g.37289G>C
NG_061543.1:g.10986G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.1293G>C MANE Select ENSP00000342007.4:p.Arg431=
ENST00000343932.4:c.1293G>C ENSP00000342007.4:p.Arg431=
NM_000761.4:c.1293G>C NP_000752.2:p.Arg431=
NM_000761.5:c.1293G>C MANE Select NP_000752.2:p.Arg431=