Linked Data
gnomAD v4:
19-38930766-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.38930766C>A , CM000681.2:g.38930766C>A | GRCh38 |
| NC_000019.9:g.39421406C>A , CM000681.1:g.39421406C>A | GRCh37 |
| NC_000019.8:g.44113246C>A | NCBI36 |
| NG_029222.1:g.5059C>A | |
| NG_031865.1:g.5131G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000221431.10:c.-30G>T (SARS2) | ENSP00000221431.5:n.-30G>T | |
| ENST00000308018.8:c.-252C>A (MRPS12) | ENSP00000308845.3:n.-252C>A | |
| ENST00000599996.1:c.476-4466G>T | ||
| NM_001145901.1:c.-30G>T (SARS2) | NP_001139373.1:n.-30G>T | |
| NM_017827.3:c.-30G>T (SARS2) | NP_060297.1:n.-30G>T | |
| NM_033362.3:c.-252C>A (MRPS12) | NP_203526.1:n.-252C>A |