Linked Data
dbSNP Id:
rs1687176453
gnomAD v4:
1-92837522-C-T
MyVariant Identifiers:
chr1:g.93303079C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.92837522C>T , CM000663.2:g.92837522C>T | GRCh38 |
| NC_000001.10:g.93303079C>T , CM000663.1:g.93303079C>T | GRCh37 |
| NC_000001.9:g.93075667C>T | NCBI36 |
| NG_011779.1:g.10486C>T | |
| NG_033051.1:g.129001G>A | |
| NG_011779.2:g.10537C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370321.8:c.594C>T (RPL5) MANE Select | ENSP00000359345.2:p.His198= | |
| ENST00000645119.1:c.324+2609C>T (RPL5) | ENSP00000493811.1:n.324+2609C>T | |
| ENST00000645300.1:c.444C>T (RPL5) | ENSP00000495589.1:p.His148= | |
| ENST00000645908.1:n.328C>T (RPL5) | ||
| ENST00000370321.7:c.594C>T (RPL5) | ENSP00000359345.2:p.His198= | |
| ENST00000497519.1:n.913C>T (RPL5) | ||
| ENST00000615519.4:c.475-4488G>A (DIPK1A) | ENSP00000483279.1:n.475-4488G>A | |
| NM_000969.3:c.594C>T (RPL5) | NP_000960.2:p.His198= | |
| NM_001252273.1:c.475-4488G>A (DIPK1A) | NP_001239202.1:n.475-4488G>A | |
| NM_000969.5:c.594C>T (RPL5) MANE Select | NP_000960.2:p.His198= | |
| NR_146333.1:n.653C>T (RPL5) | ||
| NM_001252273.2:c.475-4488G>A (DIPK1A) | NP_001239202.1:n.475-4488G>A |