Canonical Allele Identifier: CA393177351
Gene: CYP1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749893G>C , CM000677.2:g.74749893G>C GRCh38
NC_000015.9:g.75042234G>C , CM000677.1:g.75042234G>C GRCh37
NC_000015.8:g.72829287G>C NCBI36
NG_008431.1:g.32352G>C
NG_008431.2:g.32352G>C
NG_061543.1:g.6049G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.155G>C MANE Select ENSP00000342007.4:p.Gly52Ala
ENST00000343932.4:c.155G>C ENSP00000342007.4:p.Gly52Ala
NM_000761.4:c.155G>C NP_000752.2:p.Gly52Ala
NM_000761.5:c.155G>C MANE Select NP_000752.2:p.Gly52Ala