Linked Data
dbSNP Id:
rs1171219977
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.114044109C>G , CM000672.2:g.114044109C>G | GRCh38 |
| NC_000010.10:g.115803868C>G , CM000672.1:g.115803868C>G | GRCh37 |
| NC_000010.9:g.115793858C>G | NCBI36 |
| NG_012187.1:g.5063C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369295.4:c.-24C>G MANE Select | ENSP00000358301.2:n.-24C>G | |
| ENST00000369295.3:c.-24C>G | ENSP00000358301.2:n.-24C>G | |
| NM_000684.2:c.-24C>G | NP_000675.1:n.-24C>G | |
| NM_000684.3:c.-24C>G MANE Select | NP_000675.1:n.-24C>G |