Canonical Allele Identifier: CA2187827239
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755207G= , CM000677.2:g.74755207G= GRCh38
NC_000015.9:g.75047548G= , CM000677.1:g.75047548G= GRCh37
NC_000015.8:g.72834601G= NCBI36
NG_008431.1:g.37666G=
NG_008431.2:g.37666G=
NG_061543.1:g.11363G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*119G= MANE Select ENSP00000342007.4:n.*119G=
ENST00000343932.4:c.*119G= ENSP00000342007.4:n.*119G=
NM_000761.4:c.*119G= NP_000752.2:n.*119G=
NM_000761.5:c.*119G= MANE Select NP_000752.2:n.*119G=