Canonical Allele Identifier: CA2187824815
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74750278G= , CM000677.2:g.74750278G= GRCh38
NC_000015.9:g.75042619G= , CM000677.1:g.75042619G= GRCh37
NC_000015.8:g.72829672G= NCBI36
NG_008431.1:g.32737G=
NG_008431.2:g.32737G=
NG_061543.1:g.6434G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.540G= MANE Select ENSP00000342007.4:p.Met180=
ENST00000343932.4:c.540G= ENSP00000342007.4:p.Met180=
NM_000761.4:c.540G= NP_000752.2:p.Met180=
NM_000761.5:c.540G= MANE Select NP_000752.2:p.Met180=