UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Linked Data
ClinVar Variation Id:
14973
ClinVar RCV Id:
RCV000016113
dbSNP Id:
rs34907654
PubMed:
PMID:836882
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.5254680C>G , CM000673.2:g.5254680C>G | GRCh38 |
| NC_000011.9:g.5275910C>G , CM000673.1:g.5275910C>G | GRCh37 |
| NC_000011.8:g.5232486C>G | NCBI36 |
| NG_000007.3:g.42936G>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000336906.6:c.49G>C MANE Select | ENSP00000338082.4:p.Gly17Arg | |
| ENST00000380252.6:c.-73-166G>C | ENSP00000369602.2:n.-73-166G>C | |
| ENST00000380259.7:c.1595G>C | ENSP00000369609.3:n.1595G>C | |
| ENST00000642908.1:c.49G>C | ENSP00000495346.1:p.Gly17Arg | |
| ENST00000647543.1:c.49G>C | ENSP00000496470.1:p.Gly17Arg | |
| ENST00000336906.4:c.49G>C | ENSP00000338082.4:p.Gly17Arg | |
| ENST00000380252.5:c.63-166G>C | ENSP00000369602.1:n.63-166G>C | |
| ENST00000380259.6:c.49G>C | ENSP00000369609.2:p.Gly17Arg | |
| ENST00000444587.1:c.49G>C | ENSP00000488218.1:p.Gly17Arg | |
| ENST00000620888.4:c.49G>C | ENSP00000479637.1:p.Gly17Arg | |
| ENST00000624109.1:c.309C>G | ENSP00000485458.1:p.Ala103= | |
| NM_000184.2:c.49G>C | NP_000175.1:p.Gly17Arg | |
| NM_000184.3:c.49G>C MANE Select | NP_000175.1:p.Gly17Arg |