Canonical Allele Identifier: CA971501051
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs2141742497
gnomAD v3: 15-74755343-C-A
gnomAD v4: 15-74755343-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755343C>A , CM000677.2:g.74755343C>A GRCh38
NC_000015.9:g.75047684C>A , CM000677.1:g.75047684C>A GRCh37
NC_000015.8:g.72834737C>A NCBI36
NG_008431.1:g.37802C>A
NG_008431.2:g.37802C>A
NG_061543.1:g.11499C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*255C>A MANE Select ENSP00000342007.4:n.*255C>A
ENST00000343932.4:c.*255C>A ENSP00000342007.4:n.*255C>A
NM_000761.4:c.*255C>A NP_000752.2:n.*255C>A
NM_000761.5:c.*255C>A MANE Select NP_000752.2:n.*255C>A
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