Canonical Allele Identifier: CA393179196
Gene: CYP1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74750277T>A , CM000677.2:g.74750277T>A GRCh38
NC_000015.9:g.75042618T>A , CM000677.1:g.75042618T>A GRCh37
NC_000015.8:g.72829671T>A NCBI36
NG_008431.1:g.32736T>A
NG_008431.2:g.32736T>A
NG_061543.1:g.6433T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.539T>A MANE Select ENSP00000342007.4:p.Met180Lys
ENST00000343932.4:c.539T>A ENSP00000342007.4:p.Met180Lys
NM_000761.4:c.539T>A NP_000752.2:p.Met180Lys
NM_000761.5:c.539T>A MANE Select NP_000752.2:p.Met180Lys