Canonical Allele Identifier: CA2187825635
Gene: CYP1A2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74751954C= , CM000677.2:g.74751954C= GRCh38
NC_000015.9:g.75044295C= , CM000677.1:g.75044295C= GRCh37
NC_000015.8:g.72831348C= NCBI36
NG_008431.1:g.34413C=
NG_008431.2:g.34413C=
NG_061543.1:g.8110C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.1042+100C= MANE Select ENSP00000342007.4:n.1042+100C=
ENST00000343932.4:c.1042+100C= ENSP00000342007.4:n.1042+100C=
NM_000761.4:c.1042+100C= NP_000752.2:n.1042+100C=
NM_000761.5:c.1042+100C= MANE Select NP_000752.2:n.1042+100C=
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