Canonical Allele Identifier: CA2187826274
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74753237T= , CM000677.2:g.74753237T= GRCh38
NC_000015.9:g.75045578T= , CM000677.1:g.75045578T= GRCh37
NC_000015.8:g.72832631T= NCBI36
NG_008431.1:g.35696T=
NG_008431.2:g.35696T=
NG_061543.1:g.9393T=

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.1220T= MANE Select ENSP00000342007.4:p.Val407=
ENST00000343932.4:c.1220T= ENSP00000342007.4:p.Val407=
NM_000761.4:c.1220T= NP_000752.2:p.Val407=
NM_000761.5:c.1220T= MANE Select NP_000752.2:p.Val407=