Linked Data
ClinVar Variation Id:
18032
ClinVar RCV Id:
RCV000019648
dbSNP Id:
rs121909565
PubMed:
PMID:1551681
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.173909564A>G , CM000663.2:g.173909564A>G | GRCh38 |
| NC_000001.10:g.173878702A>G , CM000663.1:g.173878702A>G | GRCh37 |
| NC_000001.9:g.172145325A>G | NCBI36 |
| NG_012462.1:g.12815T>C , LRG_577:g.12815T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367698.4:c.1141T>C MANE Select | ENSP00000356671.3:p.Ser381Pro | |
| ENST00000367698.3:c.1141T>C | ENSP00000356671.3:p.Ser381Pro | |
| ENST00000617423.4:c.560-2071T>C | ENSP00000478688.1:n.560-2071T>C | |
| NM_000488.3:c.1141T>C , LRG_577t1:c.1141T>C | NP_000479.1:p.Ser381Pro | |
| XM_005245198.2:c.997T>C | XP_005245255.1:p.Ser333Pro | |
| NM_001365052.1:c.997T>C | NP_001351981.1:p.Ser333Pro | |
| NM_000488.4:c.1141T>C MANE Select | NP_000479.1:p.Ser381Pro | |
| NM_001365052.2:c.997T>C | NP_001351981.1:p.Ser333Pro | |
| NM_001386302.1:c.1264T>C | NP_001373231.1:p.Ser422Pro | |
| NM_001386303.1:c.1222T>C | NP_001373232.1:p.Ser408Pro | |
| NM_001386304.1:c.1120T>C | NP_001373233.1:p.Ser374Pro | |
| NM_001386305.1:c.1084T>C | NP_001373234.1:p.Ser362Pro | |
| NM_001386306.1:c.925T>C | NP_001373235.1:p.Ser309Pro |