Linked Data
ClinVar Variation Id:
1508176
ClinVar RCV Id:
RCV002009686
dbSNP Id:
rs2135840732
gnomAD v4:
11-64758603-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.64758603C>G , CM000673.2:g.64758603C>G | GRCh38 |
| NC_000011.9:g.64526075C>G , CM000673.1:g.64526075C>G | GRCh37 |
| NC_000011.8:g.64282651C>G | NCBI36 |
| NG_013018.1:g.7113G>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000164139.4:c.345G>C MANE Select | ENSP00000164139.3:p.Gln115His | |
| ENST00000164139.3:c.345G>C | ENSP00000164139.3:p.Gln115His | |
| ENST00000377432.7:c.244-337G>C | ENSP00000366650.3:n.244-337G>C | |
| NM_001164716.1:c.244-337G>C | NP_001158188.1:n.244-337G>C | |
| NM_005609.2:c.345G>C | NP_005600.1:p.Gln115His | |
| NM_005609.3:c.345G>C | NP_005600.1:p.Gln115His | |
| NM_005609.4:c.345G>C MANE Select | NP_005600.1:p.Gln115His |