Linked Data
gnomAD v4:
8-47960333-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.47960333G>T , CM000670.2:g.47960333G>T | GRCh38 |
| NC_000008.10:g.48872893G>T , CM000670.1:g.48872893G>T | GRCh37 |
| NC_000008.9:g.49035446G>T | NCBI36 |
| NG_023435.1:g.4851C>A , LRG_162:g.4851C>A | |
| NG_032967.1:g.5131G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000518221.5:c.-15+13G>T | ENSP00000430329.1:n.-15+13G>T | |
| NM_005914.3:c.-812G>T | NP_005905.2:n.-812G>T | |
| NM_182746.2:c.-696G>T | NP_877423.1:n.-696G>T | |
| XM_005251234.1:c.-1058G>T | XP_005251291.1:n.-1058G>T |