Canonical Allele Identifier: CA2187824836
Gene: CYP1A2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74750328C= , CM000677.2:g.74750328C= GRCh38
NC_000015.9:g.75042669C= , CM000677.1:g.75042669C= GRCh37
NC_000015.8:g.72829722C= NCBI36
NG_008431.1:g.32787C=
NG_008431.2:g.32787C=
NG_061543.1:g.6484C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.590C= MANE Select ENSP00000342007.4:p.Ala197=
ENST00000343932.4:c.590C= ENSP00000342007.4:p.Ala197=
NM_000761.4:c.590C= NP_000752.2:p.Ala197=
NM_000761.5:c.590C= MANE Select NP_000752.2:p.Ala197=
Search 100 bp 5'
Search 100 bp 3'