Canonical Allele Identifier: CA971501141
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs2063333852
gnomAD v3: 15-74755376-A-T
gnomAD v4: 15-74755376-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755376A>T , CM000677.2:g.74755376A>T GRCh38
NC_000015.9:g.75047717A>T , CM000677.1:g.75047717A>T GRCh37
NC_000015.8:g.72834770A>T NCBI36
NG_008431.1:g.37835A>T
NG_008431.2:g.37835A>T
NG_061543.1:g.11532A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*288A>T MANE Select ENSP00000342007.4:n.*288A>T
ENST00000343932.4:c.*288A>T ENSP00000342007.4:n.*288A>T
NM_000761.4:c.*288A>T NP_000752.2:n.*288A>T
NM_000761.5:c.*288A>T MANE Select NP_000752.2:n.*288A>T
Search 100 bp 5'
Search 100 bp 3'