Linked Data
gnomAD v4:
19-38930794-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.38930794C>T , CM000681.2:g.38930794C>T | GRCh38 |
| NC_000019.9:g.39421434C>T , CM000681.1:g.39421434C>T | GRCh37 |
| NC_000019.8:g.44113274C>T | NCBI36 |
| NG_029222.1:g.5087C>T | |
| NG_031865.1:g.5103G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000221431.10:c.-58G>A (SARS2) | ENSP00000221431.5:n.-58G>A | |
| ENST00000308018.8:c.-224C>T (MRPS12) | ENSP00000308845.3:n.-224C>T | |
| ENST00000599996.1:c.476-4494G>A | ||
| NM_001145901.1:c.-58G>A (SARS2) | NP_001139373.1:n.-58G>A | |
| NM_017827.3:c.-58G>A (SARS2) | NP_060297.1:n.-58G>A | |
| NM_033362.3:c.-224C>T (MRPS12) | NP_203526.1:n.-224C>T |