Canonical Allele Identifier: CA2187827059
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74754839C= , CM000677.2:g.74754839C= GRCh38
NC_000015.9:g.75047180C= , CM000677.1:g.75047180C= GRCh37
NC_000015.8:g.72834233C= NCBI36
NG_008431.1:g.37298C=
NG_008431.2:g.37298C=
NG_061543.1:g.10995C=

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.1302C= MANE Select ENSP00000342007.4:p.Thr434=
ENST00000343932.4:c.1302C= ENSP00000342007.4:p.Thr434=
NM_000761.4:c.1302C= NP_000752.2:p.Thr434=
NM_000761.5:c.1302C= MANE Select NP_000752.2:p.Thr434=