Linked Data
dbSNP Id:
rs1842252624
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.55089145A>G , CM000672.2:g.55089145A>G | GRCh38 |
| NC_000010.10:g.56848905A>G , CM000672.1:g.56848905A>G | GRCh37 |
| NC_000010.9:g.56518911A>G | NCBI36 |
| NG_009191.3:g.545038T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000458638.1:c.-80+77431T>C | ENSP00000394465.1:n.-80+77431T>C | |
| ENST00000613346.4:c.-80+77431T>C | ENSP00000481211.1:n.-80+77431T>C | |
| NM_001354404.1:c.-80+77431T>C | NP_001341333.1:n.-80+77431T>C | |
| XM_017016573.2:c.-157+77431T>C | XP_016872062.1:n.-157+77431T>C | |
| NM_001354404.2:c.-80+77431T>C | NP_001341333.1:n.-80+77431T>C |