Linked Data
ClinVar Variation Id:
6990
ClinVar RCV Id:
RCV000007406
dbSNP Id:
rs104894447
PubMed:
PMID:8808595
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.49622053A>G , CM000676.2:g.49622053A>G | GRCh38 |
| NC_000014.8:g.50088771A>G , CM000676.1:g.50088771A>G | GRCh37 |
| NC_000014.7:g.49158521A>G | NCBI36 |
| NG_008920.1:g.6283A>G | |
| NG_033054.1:g.3579T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000305386.4:c.785A>G MANE Select | ENSP00000307423.2:p.His262Arg | |
| ENST00000305386.3:c.785A>G | ENSP00000307423.2:p.His262Arg | |
| NM_002408.3:c.785A>G | NP_002399.1:p.His262Arg | |
| NM_002408.4:c.785A>G MANE Select | NP_002399.1:p.His262Arg |