Canonical Allele Identifier: CA393177378
Gene: CYP1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749899T>C , CM000677.2:g.74749899T>C GRCh38
NC_000015.9:g.75042240T>C , CM000677.1:g.75042240T>C GRCh37
NC_000015.8:g.72829293T>C NCBI36
NG_008431.1:g.32358T>C
NG_008431.2:g.32358T>C
NG_061543.1:g.6055T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.161T>C MANE Select ENSP00000342007.4:p.Val54Ala
ENST00000343932.4:c.161T>C ENSP00000342007.4:p.Val54Ala
NM_000761.4:c.161T>C NP_000752.2:p.Val54Ala
NM_000761.5:c.161T>C MANE Select NP_000752.2:p.Val54Ala