Linked Data
ClinVar Variation Id:
371995
ClinVar RCV Id:
RCV001536846
dbSNP Id:
rs1057517610
gnomAD v2:
10-88649921-C-G
gnomAD v4:
10-86890164-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.86890164C>G , CM000672.2:g.86890164C>G | GRCh38 |
| NC_000010.10:g.88649921C>G , CM000672.1:g.88649921C>G | GRCh37 |
| NC_000010.9:g.88639901C>G | NCBI36 |
| NG_009362.1:g.138526C>G , LRG_298:g.138526C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000480152.3:c.170C>G | ENSP00000483569.2:p.Pro57Arg | |
| ENST00000635816.2:c.170C>G | ENSP00000489707.1:p.Pro57Arg | |
| ENST00000636056.2:c.170C>G | ENSP00000490273.1:p.Pro57Arg | |
| ENST00000372037.8:c.170C>G MANE Select | ENSP00000361107.2:p.Pro57Arg | |
| ENST00000635816.1:c.170C>G | ENSP00000489707.1:p.Pro57Arg | |
| ENST00000636056.1:c.170C>G | ENSP00000490273.1:p.Pro57Arg | |
| ENST00000638429.1:c.170C>G | ENSP00000492290.1:p.Pro57Arg | |
| ENST00000372037.7:c.170C>G | ENSP00000361107.1:p.Pro57Arg | |
| NM_004329.2:c.170C>G , LRG_298t1:c.170C>G | NP_004320.2:p.Pro57Arg | |
| XM_011540103.1:c.170C>G | XP_011538405.1:p.Pro57Arg | |
| XM_011540104.1:c.170C>G | XP_011538406.1:p.Pro57Arg | |
| XM_011540103.2:c.170C>G | XP_011538405.1:p.Pro57Arg | |
| XM_011540104.2:c.170C>G | XP_011538406.1:p.Pro57Arg | |
| NM_004329.3:c.170C>G MANE Select | NP_004320.2:p.Pro57Arg |