Linked Data
dbSNP Id:
rs943217969
gnomAD v4:
5-82276671-G-C
MyVariant Identifiers:
chr5:g.81572490G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.82276671G>C , CM000667.2:g.82276671G>C | GRCh38 |
| NC_000005.9:g.81572490G>C , CM000667.1:g.81572490G>C | GRCh37 |
| NC_000005.8:g.81608246G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000296674.13:c.165-153C>G (RPS23) MANE Select | ENSP00000296674.8:n.165-153C>G | |
| ENST00000651545.1:c.165-153C>G (RPS23) | ENSP00000498621.1:n.165-153C>G | |
| ENST00000296674.12:c.165-153C>G (RPS23) | ENSP00000296674.8:n.165-153C>G | |
| ENST00000503605.1:n.374-153C>G (RPS23) | ||
| ENST00000504293.5:n.260-153C>G (RPS23) | ||
| ENST00000507980.1:c.165-153C>G (RPS23) | ENSP00000422071.1:n.165-153C>G | |
| ENST00000510019.5:c.165-153C>G (RPS23) | ENSP00000425833.1:n.165-153C>G | |
| ENST00000510210.5:c.165-153C>G (RPS23) | ENSP00000427043.1:n.165-153C>G | |
| ENST00000512493.5:c.165-153C>G (RPS23) | ENSP00000425865.1:n.165-153C>G | |
| ENST00000514253.2:n.718G>C (ATG10) | ||
| NM_001025.4:c.165-153C>G (RPS23) | NP_001016.1:n.165-153C>G | |
| NM_001025.5:c.165-153C>G (RPS23) MANE Select | NP_001016.1:n.165-153C>G |