Canonical Allele Identifier: CA2187825723
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74752156C= , CM000677.2:g.74752156C= GRCh38
NC_000015.9:g.75044497C= , CM000677.1:g.75044497C= GRCh37
NC_000015.8:g.72831550C= NCBI36
NG_008431.1:g.34615C=
NG_008431.2:g.34615C=
NG_061543.1:g.8312C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.1075C= MANE Select ENSP00000342007.4:p.Leu359=
ENST00000343932.4:c.1075C= ENSP00000342007.4:p.Leu359=
NM_000761.4:c.1075C= NP_000752.2:p.Leu359=
NM_000761.5:c.1075C= MANE Select NP_000752.2:p.Leu359=