Canonical Allele Identifier: CA971501078
Gene: CYP1A2 HGNC NCBI

Linked Data

gnomAD v3: 15-74755351-A-T
gnomAD v4: 15-74755351-A-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755351A>T , CM000677.2:g.74755351A>T GRCh38
NC_000015.9:g.75047692A>T , CM000677.1:g.75047692A>T GRCh37
NC_000015.8:g.72834745A>T NCBI36
NG_008431.1:g.37810A>T
NG_008431.2:g.37810A>T
NG_061543.1:g.11507A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*263A>T MANE Select ENSP00000342007.4:n.*263A>T
ENST00000343932.4:c.*263A>T ENSP00000342007.4:n.*263A>T
NM_000761.4:c.*263A>T NP_000752.2:n.*263A>T
NM_000761.5:c.*263A>T MANE Select NP_000752.2:n.*263A>T
Search 100 bp 5'
Search 100 bp 3'