Canonical Allele Identifier: CA971501067
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs1596359535
gnomAD v3: 15-74755349-T-C
gnomAD v4: 15-74755349-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755349T>C , CM000677.2:g.74755349T>C GRCh38
NC_000015.9:g.75047690T>C , CM000677.1:g.75047690T>C GRCh37
NC_000015.8:g.72834743T>C NCBI36
NG_008431.1:g.37808T>C
NG_008431.2:g.37808T>C
NG_061543.1:g.11505T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*261T>C MANE Select ENSP00000342007.4:n.*261T>C
ENST00000343932.4:c.*261T>C ENSP00000342007.4:n.*261T>C
NM_000761.4:c.*261T>C NP_000752.2:n.*261T>C
NM_000761.5:c.*261T>C MANE Select NP_000752.2:n.*261T>C
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