Canonical Allele Identifier: CA2187827026
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74754771C= , CM000677.2:g.74754771C= GRCh38
NC_000015.9:g.75047112C= , CM000677.1:g.75047112C= GRCh37
NC_000015.8:g.72834165C= NCBI36
NG_008431.1:g.37230C=
NG_008431.2:g.37230C=
NG_061543.1:g.10927C=

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.1254-20C= MANE Select ENSP00000342007.4:n.1254-20C=
ENST00000343932.4:c.1254-20C= ENSP00000342007.4:n.1254-20C=
NM_000761.4:c.1254-20C= NP_000752.2:n.1254-20C=
NM_000761.5:c.1254-20C= MANE Select NP_000752.2:n.1254-20C=