Linked Data
dbSNP Id:
rs13024811
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.38753089T>G , CM000664.2:g.38753089T>G | GRCh38 |
| NC_000002.11:g.38980231T>G , CM000664.1:g.38980231T>G | GRCh37 |
| NC_000002.10:g.38833735T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000409011.5:c.-281+1271T>G | ENSP00000387191.1:n.-281+1271T>G |