Linked Data
ClinVar Variation Id:
11910
ClinVar RCV Id:
RCV001267070
dbSNP Id:
rs121965021
ExAC:
4:997206 C / G
gnomAD v2:
4-997206-C-G
gnomAD v3:
4-1003418-C-G
gnomAD v4:
4-1003418-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.1003418C>G , CM000666.2:g.1003418C>G | GRCh38 |
| NC_000004.11:g.997206C>G , CM000666.1:g.997206C>G | GRCh37 |
| NC_000004.10:g.987206C>G | NCBI36 |
| NG_008103.1:g.21422C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000247933.9:c.1598C>G | ENSP00000247933.4:p.Pro533Arg | |
| ENST00000514224.2:c.1598C>G MANE Select | ENSP00000425081.2:p.Pro533Arg | |
| ENST00000652070.1:n.1654C>G | ||
| ENST00000247933.8:c.1598C>G | ENSP00000247933.4:p.Pro533Arg | |
| ENST00000514224.1:c.1202C>G | ENSP00000425081.1:p.Pro401Arg | |
| ENST00000514698.5:n.1705C>G | ||
| NM_000203.4:c.1598C>G | NP_000194.2:p.Pro533Arg | |
| NR_110313.1:n.1686C>G | ||
| XM_006713882.2:c.1202C>G | XP_006713945.1:p.Pro401Arg | |
| XM_011513459.1:c.1664C>G | XP_011511761.1:p.Pro555Arg | |
| XM_011513460.1:c.1457C>G | XP_011511762.1:p.Pro486Arg | |
| XM_011513461.1:c.1391C>G | XP_011511763.1:p.Pro464Arg | |
| XM_011513462.1:c.1310C>G | XP_011511764.1:p.Pro437Arg | |
| XM_011513463.1:c.1310C>G | XP_011511765.1:p.Pro437Arg | |
| XR_924947.1:n.1854C>G | ||
| NM_000203.5:c.1598C>G MANE Select | NP_000194.2:p.Pro533Arg | |
| NM_001363576.1:c.1202C>G | NP_001350505.1:p.Pro401Arg | |
| XM_011513461.2:c.1391C>G | XP_011511763.1:p.Pro464Arg | |
| XM_017008163.1:c.638C>G | XP_016863652.1:p.Pro213Arg |