Linked Data
dbSNP Id:
rs1865722536
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.67483020C>T , CM000673.2:g.67483020C>T | GRCh38 |
| NC_000011.9:g.67250491C>T , CM000673.1:g.67250491C>T | GRCh37 |
| NC_000011.8:g.67007067C>T | NCBI36 |
| NG_008969.1:g.4987C>T , LRG_460:g.4987C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682699.1:c.-139C>T | ENSP00000507935.1:n.-139C>T | |
| XM_024448761.1:c.-139C>T | XP_024304529.1:n.-139C>T |