Canonical Allele Identifier: CA2187827269
Gene: CYP1A2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755301C= , CM000677.2:g.74755301C= GRCh38
NC_000015.9:g.75047642C= , CM000677.1:g.75047642C= GRCh37
NC_000015.8:g.72834695C= NCBI36
NG_008431.1:g.37760C=
NG_008431.2:g.37760C=
NG_061543.1:g.11457C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*213C= MANE Select ENSP00000342007.4:n.*213C=
ENST00000343932.4:c.*213C= ENSP00000342007.4:n.*213C=
NM_000761.4:c.*213C= NP_000752.2:n.*213C=
NM_000761.5:c.*213C= MANE Select NP_000752.2:n.*213C=
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