Linked Data
ClinVar Variation Id:
1474491
ClinVar RCV Id:
RCV001973418
dbSNP Id:
rs1387833836
gnomAD v2:
10-112572193-C-T
gnomAD v4:
10-110812435-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.110812435C>T , CM000672.2:g.110812435C>T | GRCh38 |
| NC_000010.10:g.112572193C>T , CM000672.1:g.112572193C>T | GRCh37 |
| NC_000010.9:g.112562183C>T | NCBI36 |
| NG_021177.1:g.173039C>T , LRG_382:g.173039C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369519.4:c.2038C>T MANE Select | ENSP00000358532.3:p.Pro680Ser | |
| ENST00000369519.3:c.2038C>T | ENSP00000358532.3:p.Pro680Ser | |
| NM_001134363.2:c.2038C>T | NP_001127835.2:p.Pro680Ser | |
| XM_011539697.1:c.1654C>T | XP_011537999.1:p.Pro552Ser | |
| XM_017016103.2:c.1873C>T | XP_016871592.1:p.Pro625Ser | |
| XM_017016104.2:c.1654C>T | XP_016871593.1:p.Pro552Ser | |
| NM_001134363.3:c.2038C>T MANE Select | NP_001127835.2:p.Pro680Ser |