Linked Data
gnomAD v4:
18-24460633-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.24460633G>T , CM000680.2:g.24460633G>T | GRCh38 |
| NC_000018.9:g.22040597G>T , CM000680.1:g.22040597G>T | GRCh37 |
| NC_000018.8:g.20294595G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000256906.4:c.-96G>T | ENSP00000256906.4:n.-96G>T | |
| NM_001143828.1:c.-96G>T | NP_001137300.1:n.-96G>T | |
| NM_001160166.1:c.-96G>T | NP_001153638.1:n.-96G>T | |
| NM_021624.3:c.-96G>T | NP_067637.2:n.-96G>T | |
| XM_011526133.1:c.-96G>T | XP_011524435.1:n.-96G>T | |
| XM_011526134.1:c.-96G>T | XP_011524436.1:n.-96G>T |