Linked Data
dbSNP Id:
rs1022383626
gnomAD v4:
19-38930807-C-G
MyVariant Identifiers:
chr19:g.38930807C>G (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.38930807C>G , CM000681.2:g.38930807C>G | GRCh38 |
| NC_000019.9:g.39421447C>G , CM000681.1:g.39421447C>G | GRCh37 |
| NC_000019.8:g.44113287C>G | NCBI36 |
| NG_029222.1:g.5100C>G | |
| NG_031865.1:g.5090G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000221431.10:c.-71G>C (SARS2) | ENSP00000221431.5:n.-71G>C | |
| ENST00000308018.8:c.-211C>G (MRPS12) | ENSP00000308845.3:n.-211C>G | |
| ENST00000599996.1:c.476-4507G>C | ||
| NM_001145901.1:c.-71G>C (SARS2) | NP_001139373.1:n.-71G>C | |
| NM_017827.3:c.-71G>C (SARS2) | NP_060297.1:n.-71G>C | |
| NM_033362.3:c.-211C>G (MRPS12) | NP_203526.1:n.-211C>G |