Linked Data
gnomAD v4:
X-48683792-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.48683792G>T , CM000685.2:g.48683792G>T | GRCh38 |
| NC_000023.10:g.48542181G>T , CM000685.1:g.48542181G>T | GRCh37 |
| NC_000023.9:g.48427125G>T | NCBI36 |
| NG_007877.1:g.4996G>T , LRG_125:g.4996G>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000698625.1:c.-34-28G>T | ENSP00000513844.1:n.-34-28G>T | |
| ENST00000376701.4:c.-62G>T | ENSP00000365891.4:n.-62G>T | |
| ENST00000450772.5:c.-34-28G>T | ENSP00000410537.1:n.-34-28G>T | |
| XM_011543977.1:c.-62G>T | XP_011542279.1:n.-62G>T | |
| XM_011543977.2:c.-62G>T | XP_011542279.1:n.-62G>T | |
| XM_017029786.1:c.-62G>T | XP_016885275.1:n.-62G>T |