Linked Data
ClinVar Variation Id:
4621
ClinVar RCV Id:
RCV000004884
dbSNP Id:
rs111033576
PubMed:
PMID:11431692
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.100989271G>C , CM000672.2:g.100989271G>C | GRCh38 |
| NC_000010.10:g.102749028G>C , CM000672.1:g.102749028G>C | GRCh37 |
| NC_000010.9:g.102739018G>C | NCBI36 |
| NG_011646.1:g.3245C>G | |
| NG_012624.1:g.6736G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000311916.8:c.1061G>C MANE Select | ENSP00000309595.2:p.Arg354Pro | |
| ENST00000370228.2:c.1061G>C | ENSP00000359248.1:p.Arg354Pro | |
| ENST00000643860.1:c.1061G>C | ENSP00000494389.1:p.Arg354Pro | |
| ENST00000646226.1:n.59-373G>C | ||
| ENST00000650396.1:c.84G>C | ||
| ENST00000311916.6:c.1061G>C | ENSP00000309595.2:p.Arg354Pro | |
| ENST00000370228.1:c.1061G>C | ENSP00000359248.1:p.Arg354Pro | |
| ENST00000459764.1:n.87-373G>C | ||
| ENST00000473656.5:n.65-373G>C | ||
| ENST00000476766.5:n.192-435G>C | ||
| NM_001163812.1:c.1061G>C | NP_001157284.1:p.Arg354Pro | |
| NM_001163813.1:c.-119-373G>C | NP_001157285.1:n.-119-373G>C | |
| NM_001163814.1:c.-119-373G>C | NP_001157286.1:n.-119-373G>C | |
| NM_021830.4:c.1061G>C | NP_068602.2:p.Arg354Pro | |
| XM_011539975.1:c.-57-435G>C | XP_011538277.1:n.-57-435G>C | |
| XR_945788.1:n.1894G>C | ||
| XM_011539975.2:c.-57-435G>C | XP_011538277.1:n.-57-435G>C | |
| XM_017016437.1:c.-240G>C | XP_016871926.1:n.-240G>C | |
| XR_001747142.1:n.1235G>C | ||
| XR_001747144.1:n.1235G>C | ||
| XR_002956991.1:n.1235G>C | ||
| XR_945788.2:n.1235G>C | ||
| NM_021830.5:c.1061G>C MANE Select | NP_068602.2:p.Arg354Pro | |
| NM_001163812.2:c.1061G>C | NP_001157284.1:p.Arg354Pro | |
| NM_001163813.2:c.-119-373G>C | NP_001157285.1:n.-119-373G>C | |
| NM_001163814.2:c.-119-373G>C | NP_001157286.1:n.-119-373G>C | |
| NM_001368275.1:c.-57-435G>C | NP_001355204.1:n.-57-435G>C | |
| NR_160738.1:n.1729G>C | ||
| NR_160739.1:n.72-373G>C | ||
| NR_160740.1:n.1729G>C | ||
| NR_160741.1:n.1729G>C | ||
| NR_160742.1:n.1729G>C |