Canonical Allele Identifier: CA393178500
Gene: CYP1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74750108A>T , CM000677.2:g.74750108A>T GRCh38
NC_000015.9:g.75042449A>T , CM000677.1:g.75042449A>T GRCh37
NC_000015.8:g.72829502A>T NCBI36
NG_008431.1:g.32567A>T
NG_008431.2:g.32567A>T
NG_061543.1:g.6264A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.370A>T MANE Select ENSP00000342007.4:p.Thr124Ser
ENST00000343932.4:c.370A>T ENSP00000342007.4:p.Thr124Ser
NM_000761.4:c.370A>T NP_000752.2:p.Thr124Ser
NM_000761.5:c.370A>T MANE Select NP_000752.2:p.Thr124Ser