Linked Data
gnomAD v4:
19-38930798-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.38930798G>T , CM000681.2:g.38930798G>T | GRCh38 |
| NC_000019.9:g.39421438G>T , CM000681.1:g.39421438G>T | GRCh37 |
| NC_000019.8:g.44113278G>T | NCBI36 |
| NG_029222.1:g.5091G>T | |
| NG_031865.1:g.5099C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000221431.10:c.-62C>A (SARS2) | ENSP00000221431.5:n.-62C>A | |
| ENST00000308018.8:c.-220G>T (MRPS12) | ENSP00000308845.3:n.-220G>T | |
| ENST00000599996.1:c.476-4498C>A | ||
| NM_001145901.1:c.-62C>A (SARS2) | NP_001139373.1:n.-62C>A | |
| NM_017827.3:c.-62C>A (SARS2) | NP_060297.1:n.-62C>A | |
| NM_033362.3:c.-220G>T (MRPS12) | NP_203526.1:n.-220G>T |