Canonical Allele Identifier: CA2629504187
Gene: CYP1A2 HGNC NCBI

Linked Data

gnomAD v4: 15-74749622-G-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749622G>T , CM000677.2:g.74749622G>T GRCh38
NC_000015.9:g.75041963G>T , CM000677.1:g.75041963G>T GRCh37
NC_000015.8:g.72829016G>T NCBI36
NG_008431.1:g.32081G>T
NG_008431.2:g.32081G>T
NG_061543.1:g.5778G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.-9-108G>T MANE Select ENSP00000342007.4:n.-9-108G>T
ENST00000343932.4:c.-9-108G>T ENSP00000342007.4:n.-9-108G>T
NM_000761.4:c.-9-108G>T NP_000752.2:n.-9-108G>T
NM_000761.5:c.-9-108G>T MANE Select NP_000752.2:n.-9-108G>T
Search 100 bp 5'
Search 100 bp 3'