Canonical Allele Identifier: CA393179335
Gene: CYP1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74750324G>A , CM000677.2:g.74750324G>A GRCh38
NC_000015.9:g.75042665G>A , CM000677.1:g.75042665G>A GRCh37
NC_000015.8:g.72829718G>A NCBI36
NG_008431.1:g.32783G>A
NG_008431.2:g.32783G>A
NG_061543.1:g.6480G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.586G>A MANE Select ENSP00000342007.4:p.Val196Met
ENST00000343932.4:c.586G>A ENSP00000342007.4:p.Val196Met
NM_000761.4:c.586G>A NP_000752.2:p.Val196Met
NM_000761.5:c.586G>A MANE Select NP_000752.2:p.Val196Met