Canonical Allele Identifier: CA2187826959
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74754639A= , CM000677.2:g.74754639A= GRCh38
NC_000015.9:g.75046980A= , CM000677.1:g.75046980A= GRCh37
NC_000015.8:g.72834033A= NCBI36
NG_008431.1:g.37098A=
NG_008431.2:g.37098A=
NG_061543.1:g.10795A=

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.1254-152A= MANE Select ENSP00000342007.4:n.1254-152A=
ENST00000343932.4:c.1254-152A= ENSP00000342007.4:n.1254-152A=
NM_000761.4:c.1254-152A= NP_000752.2:n.1254-152A=
NM_000761.5:c.1254-152A= MANE Select NP_000752.2:n.1254-152A=