Canonical Allele Identifier: CA2187827053
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74754829G= , CM000677.2:g.74754829G= GRCh38
NC_000015.9:g.75047170G= , CM000677.1:g.75047170G= GRCh37
NC_000015.8:g.72834223G= NCBI36
NG_008431.1:g.37288G=
NG_008431.2:g.37288G=
NG_061543.1:g.10985G=

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.1292G= MANE Select ENSP00000342007.4:p.Arg431=
ENST00000343932.4:c.1292G= ENSP00000342007.4:p.Arg431=
NM_000761.4:c.1292G= NP_000752.2:p.Arg431=
NM_000761.5:c.1292G= MANE Select NP_000752.2:p.Arg431=