Linked Data
ClinVar Variation Id:
1672501
ClinVar RCV Id:
RCV002201713
dbSNP Id:
rs2102656098
MyVariant Identifiers:
chr1:g.216498854G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.216325512G>A , CM000663.2:g.216325512G>A | GRCh38 |
| NC_000001.10:g.216498854G>A , CM000663.1:g.216498854G>A | GRCh37 |
| NC_000001.9:g.214565477G>A | NCBI36 |
| NG_009497.1:g.102885C>T | |
| NG_009497.2:g.102937C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307340.8:c.936C>T MANE Select | ENSP00000305941.3:p.His312= | |
| ENST00000674083.1:c.936C>T | ENSP00000501296.1:p.His312= | |
| ENST00000307340.7:c.936C>T | ENSP00000305941.3:p.His312= | |
| ENST00000366942.3:c.936C>T | ENSP00000355909.3:p.His312= | |
| NM_007123.5:c.936C>T | NP_009054.5:p.His312= | |
| NM_206933.2:c.936C>T | NP_996816.2:p.His312= | |
| NM_206933.3:c.936C>T | NP_996816.2:p.His312= | |
| NM_007123.6:c.936C>T | NP_009054.6:p.His312= | |
| NM_206933.4:c.936C>T MANE Select | NP_996816.3:p.His312= |