Linked Data
gnomAD v4:
5-70049635-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.70049635G>C , CM000667.2:g.70049635G>C | GRCh38 |
| NC_000005.9:g.69345462G>C , CM000667.1:g.69345462G>C | GRCh37 |
| NC_000005.8:g.69381218G>C | NCBI36 |
| NG_008728.1:g.5113G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000380743.8:c.-51G>C | ENSP00000370119.4:n.-51G>C | |
| NM_017411.3:c.-51G>C | NP_059107.1:n.-51G>C | |
| NM_022875.2:c.-51G>C | NP_075013.1:n.-51G>C | |
| NM_022876.2:c.-51G>C | NP_075014.1:n.-51G>C | |
| NM_022877.2:c.-51G>C | NP_075015.1:n.-51G>C | |
| XM_011543602.1:c.-51G>C | XP_011541904.1:n.-51G>C | |
| XM_011543603.1:c.-51G>C | XP_011541905.1:n.-51G>C | |
| XR_948432.1:n.1054+61631G>C | ||
| XM_011543602.3:c.-51G>C | XP_011541904.1:n.-51G>C | |
| XM_011543603.3:c.-51G>C | XP_011541905.1:n.-51G>C |