Canonical Allele Identifier: CA2187824766
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74750159C= , CM000677.2:g.74750159C= GRCh38
NC_000015.9:g.75042500C= , CM000677.1:g.75042500C= GRCh37
NC_000015.8:g.72829553C= NCBI36
NG_008431.1:g.32618C=
NG_008431.2:g.32618C=
NG_061543.1:g.6315C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.421C= MANE Select ENSP00000342007.4:p.Gln141=
ENST00000343932.4:c.421C= ENSP00000342007.4:p.Gln141=
NM_000761.4:c.421C= NP_000752.2:p.Gln141=
NM_000761.5:c.421C= MANE Select NP_000752.2:p.Gln141=