Canonical Allele Identifier: CA393169293
Gene: CYP1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74754840G>A , CM000677.2:g.74754840G>A GRCh38
NC_000015.9:g.75047181G>A , CM000677.1:g.75047181G>A GRCh37
NC_000015.8:g.72834234G>A NCBI36
NG_008431.1:g.37299G>A
NG_008431.2:g.37299G>A
NG_061543.1:g.10996G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.1303G>A MANE Select ENSP00000342007.4:p.Ala435Thr
ENST00000343932.4:c.1303G>A ENSP00000342007.4:p.Ala435Thr
NM_000761.4:c.1303G>A NP_000752.2:p.Ala435Thr
NM_000761.5:c.1303G>A MANE Select NP_000752.2:p.Ala435Thr