Canonical Allele Identifier: CA2187824641
Gene: CYP1A2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749904A= , CM000677.2:g.74749904A= GRCh38
NC_000015.9:g.75042245A= , CM000677.1:g.75042245A= GRCh37
NC_000015.8:g.72829298A= NCBI36
NG_008431.1:g.32363A=
NG_008431.2:g.32363A=
NG_061543.1:g.6060A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.166A= MANE Select ENSP00000342007.4:p.Thr56=
ENST00000343932.4:c.166A= ENSP00000342007.4:p.Thr56=
NM_000761.4:c.166A= NP_000752.2:p.Thr56=
NM_000761.5:c.166A= MANE Select NP_000752.2:p.Thr56=
Search 100 bp 5'
Search 100 bp 3'