Canonical Allele Identifier: CA971501168
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs1212135311
gnomAD v3: 15-74755384-T-G
gnomAD v4: 15-74755384-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755384T>G , CM000677.2:g.74755384T>G GRCh38
NC_000015.9:g.75047725T>G , CM000677.1:g.75047725T>G GRCh37
NC_000015.8:g.72834778T>G NCBI36
NG_008431.1:g.37843T>G
NG_008431.2:g.37843T>G
NG_061543.1:g.11540T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*296T>G MANE Select ENSP00000342007.4:n.*296T>G
ENST00000343932.4:c.*296T>G ENSP00000342007.4:n.*296T>G
NM_000761.4:c.*296T>G NP_000752.2:n.*296T>G
NM_000761.5:c.*296T>G MANE Select NP_000752.2:n.*296T>G
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