Linked Data
ClinVar Variation Id:
1781705
ClinVar RCV Id:
RCV002415122
dbSNP Id:
rs371511223
gnomAD v3:
2-43877676-C-G
gnomAD v4:
2-43877676-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.43877676C>G , CM000664.2:g.43877676C>G | GRCh38 |
| NC_000002.11:g.44104815C>G , CM000664.1:g.44104815C>G | GRCh37 |
| NC_000002.10:g.43958319C>G | NCBI36 |
| NG_008884.1:g.43713C>G | |
| NG_008884.2:g.50735C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000272286.4:c.1872C>G MANE Select | ENSP00000272286.2:p.Val624= | |
| ENST00000272286.2:c.1872C>G | ENSP00000272286.2:p.Val624= | |
| NM_022437.2:c.1872C>G | NP_071882.1:p.Val624= | |
| XM_005264483.2:c.1869C>G | XP_005264540.1:p.Val623= | |
| XM_011533029.1:c.1884C>G | XP_011531331.1:p.Val628= | |
| XM_011533030.1:c.1881C>G | XP_011531332.1:p.Val627= | |
| XM_011533031.1:c.1656C>G | XP_011531333.1:p.Val552= | |
| XR_939707.1:n.2374C>G | ||
| NM_001357321.1:c.1869C>G | NP_001344250.1:p.Val623= | |
| XM_011533029.2:c.1884C>G | XP_011531331.1:p.Val628= | |
| XM_011533030.2:c.1881C>G | XP_011531332.1:p.Val627= | |
| XR_001738891.1:n.2388C>G | ||
| XR_939707.2:n.2388C>G | ||
| NM_022437.3:c.1872C>G MANE Select | NP_071882.1:p.Val624= | |
| NM_001357321.2:c.1869C>G | NP_001344250.1:p.Val623= |