Canonical Allele Identifier: CA2187827206
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755120G= , CM000677.2:g.74755120G= GRCh38
NC_000015.9:g.75047461G= , CM000677.1:g.75047461G= GRCh37
NC_000015.8:g.72834514G= NCBI36
NG_008431.1:g.37579G=
NG_008431.2:g.37579G=
NG_061543.1:g.11276G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*32G= MANE Select ENSP00000342007.4:n.*32G=
ENST00000343932.4:c.*32G= ENSP00000342007.4:n.*32G=
NM_000761.4:c.*32G= NP_000752.2:n.*32G=
NM_000761.5:c.*32G= MANE Select NP_000752.2:n.*32G=