Linked Data
ClinVar Variation Id:
5079
ClinVar RCV Id:
RCV000005384
dbSNP Id:
rs121917826
gnomAD v4:
16-75479552-G-T
PubMed:
PMID:15013869
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.75479552G>T , CM000678.2:g.75479552G>T | GRCh38 |
| NC_000016.9:g.75513450G>T , CM000678.1:g.75513450G>T | GRCh37 |
| NC_000016.8:g.74070951G>T | NCBI36 |
| NG_016442.1:g.20477C>A | |
| NG_016442.2:g.20890C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000332272.9:c.277C>A MANE Select | ENSP00000328983.4:p.Arg93Ser | |
| ENST00000390664.3:c.277C>A | ENSP00000375079.2:p.Arg93Ser | |
| ENST00000649341.1:c.277C>A | ENSP00000497635.1:p.Arg93Ser | |
| ENST00000649824.1:c.277C>A | ENSP00000496806.1:p.Arg93Ser | |
| ENST00000332272.8:c.277C>A | ENSP00000328983.4:p.Arg93Ser | |
| ENST00000390664.2:c.277C>A | ENSP00000375079.2:p.Arg93Ser | |
| NM_021615.4:c.277C>A | NP_067628.1:p.Arg93Ser | |
| XM_005255955.3:c.277C>A | XP_005256012.1:p.Arg93Ser | |
| XM_011523085.1:c.277C>A | XP_011521387.1:p.Arg93Ser | |
| NM_021615.5:c.277C>A MANE Select | NP_067628.1:p.Arg93Ser | |
| XM_005255955.5:c.277C>A | XP_005256012.1:p.Arg93Ser | |
| XM_011523085.3:c.277C>A | XP_011521387.1:p.Arg93Ser | |
| NR_163480.1:n.733+2265C>A | ||
| NR_163481.1:n.577+2265C>A |