Canonical Allele Identifier: CA2187824768
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74750165G= , CM000677.2:g.74750165G= GRCh38
NC_000015.9:g.75042506G= , CM000677.1:g.75042506G= GRCh37
NC_000015.8:g.72829559G= NCBI36
NG_008431.1:g.32624G=
NG_008431.2:g.32624G=
NG_061543.1:g.6321G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.427G= MANE Select ENSP00000342007.4:p.Ala143=
ENST00000343932.4:c.427G= ENSP00000342007.4:p.Ala143=
NM_000761.4:c.427G= NP_000752.2:p.Ala143=
NM_000761.5:c.427G= MANE Select NP_000752.2:p.Ala143=