Canonical Allele Identifier: CA2629504222
Gene: CYP1A2 HGNC NCBI

Linked Data

gnomAD v4: 15-74749630-G-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749630G>A , CM000677.2:g.74749630G>A GRCh38
NC_000015.9:g.75041971G>A , CM000677.1:g.75041971G>A GRCh37
NC_000015.8:g.72829024G>A NCBI36
NG_008431.1:g.32089G>A
NG_008431.2:g.32089G>A
NG_061543.1:g.5786G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.-9-100G>A MANE Select ENSP00000342007.4:n.-9-100G>A
ENST00000343932.4:c.-9-100G>A ENSP00000342007.4:n.-9-100G>A
NM_000761.4:c.-9-100G>A NP_000752.2:n.-9-100G>A
NM_000761.5:c.-9-100G>A MANE Select NP_000752.2:n.-9-100G>A
Search 100 bp 5'
Search 100 bp 3'