Linked Data
ClinVar Variation Id:
869321
ClinVar RCV Id:
RCV001078384
dbSNP Id:
rs1135071
gnomAD v4:
11-5226799-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.5226799C>G , CM000673.2:g.5226799C>G | GRCh38 |
| NC_000011.9:g.5248029C>G , CM000673.1:g.5248029C>G | GRCh37 |
| NC_000011.8:g.5204605C>G | NCBI36 |
| NG_000007.3:g.70817G>C | |
| NG_059281.1:g.5273G>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000647020.1:c.93G>C | ENSP00000494175.1:p.Arg31Ser | |
| ENST00000335295.4:c.93G>C MANE Select | ENSP00000333994.3:p.Arg31Ser | |
| ENST00000380315.2:c.93G>C | ENSP00000369671.2:p.Arg31Ser | |
| ENST00000475226.1:n.25G>C | ||
| ENST00000485743.1:n.144G>C | ||
| ENST00000633227.1:c.77G>C | ENSP00000488004.1:p.Gly26Ala | |
| NM_000518.4:c.93G>C | NP_000509.1:p.Arg31Ser | |
| NM_000518.5:c.93G>C MANE Select | NP_000509.1:p.Arg31Ser |