Canonical Allele Identifier: CA971498145
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs2063303101
gnomAD v3: 15-74749379-T-C
gnomAD v4: 15-74749379-T-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749379T>C , CM000677.2:g.74749379T>C GRCh38
NC_000015.9:g.75041720T>C , CM000677.1:g.75041720T>C GRCh37
NC_000015.8:g.72828773T>C NCBI36
NG_008431.1:g.31838T>C
NG_008431.2:g.31838T>C
NG_061543.1:g.5535T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.-9-351T>C MANE Select ENSP00000342007.4:n.-9-351T>C
ENST00000343932.4:c.-9-351T>C ENSP00000342007.4:n.-9-351T>C
NM_000761.4:c.-9-351T>C NP_000752.2:n.-9-351T>C
NM_000761.5:c.-9-351T>C MANE Select NP_000752.2:n.-9-351T>C
Search 100 bp 5'
Search 100 bp 3'