Linked Data
gnomAD v4:
2-27323152-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.27323152A>T , CM000664.2:g.27323152A>T | GRCh38 |
| NC_000002.11:g.27546019A>T , CM000664.1:g.27546019A>T | GRCh37 |
| NC_000002.10:g.27399523A>T | NCBI36 |
| NG_008075.1:g.4413T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000357186.10:c.18+1281T>A | ENSP00000349713.6:n.18+1281T>A | |
| XM_005264327.2:c.-230T>A | XP_005264384.1:n.-230T>A |