Linked Data
dbSNP Id:
rs1450760480
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.71785005C>T , CM000666.2:g.71785005C>T | GRCh38 |
| NC_000004.11:g.72650722C>T , CM000666.1:g.72650722C>T | GRCh37 |
| NC_000004.10:g.72869586C>T | NCBI36 |
| NG_012837.2:g.25516G>A | |
| NG_012837.3:g.25516G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000504199.5:c.22-951G>A | ENSP00000421725.1:n.22-951G>A | |
| ENST00000506245.1:c.-37+915G>A | ENSP00000426718.1:n.-37+915G>A | |
| NM_001204306.1:c.-36-951G>A | NP_001191235.1:n.-36-951G>A | |
| NM_001204307.1:c.22-951G>A | NP_001191236.1:n.22-951G>A |