Linked Data
ClinVar Variation Id:
4973
ClinVar RCV Id:
RCV000005261
dbSNP Id:
rs137852992
gnomAD v3:
2-43877591-T-G
gnomAD v4:
2-43877591-T-G
PubMed:
PMID:11099417
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.43877591T>G , CM000664.2:g.43877591T>G | GRCh38 |
| NC_000002.11:g.44104730T>G , CM000664.1:g.44104730T>G | GRCh37 |
| NC_000002.10:g.43958234T>G | NCBI36 |
| NG_008884.1:g.43628T>G | |
| NG_008884.2:g.50650T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000272286.4:c.1787T>G MANE Select | ENSP00000272286.2:p.Leu596Arg | |
| ENST00000272286.2:c.1787T>G | ENSP00000272286.2:p.Leu596Arg | |
| NM_022437.2:c.1787T>G | NP_071882.1:p.Leu596Arg | |
| XM_005264483.2:c.1784T>G | XP_005264540.1:p.Leu595Arg | |
| XM_011533029.1:c.1799T>G | XP_011531331.1:p.Leu600Arg | |
| XM_011533030.1:c.1796T>G | XP_011531332.1:p.Leu599Arg | |
| XM_011533031.1:c.1571T>G | XP_011531333.1:p.Leu524Arg | |
| XR_939707.1:n.2289T>G | ||
| NM_001357321.1:c.1784T>G | NP_001344250.1:p.Leu595Arg | |
| XM_011533029.2:c.1799T>G | XP_011531331.1:p.Leu600Arg | |
| XM_011533030.2:c.1796T>G | XP_011531332.1:p.Leu599Arg | |
| XR_001738891.1:n.2303T>G | ||
| XR_939707.2:n.2303T>G | ||
| NM_022437.3:c.1787T>G MANE Select | NP_071882.1:p.Leu596Arg | |
| NM_001357321.2:c.1784T>G | NP_001344250.1:p.Leu595Arg |