Linked Data
dbSNP Id:
rs537726950
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.60649486T>A , CM000676.2:g.60649486T>A | GRCh38 |
| NC_000014.8:g.61116204T>A , CM000676.1:g.61116204T>A | GRCh37 |
| NC_000014.7:g.60185957T>A | NCBI36 |
| NG_008231.1:g.4952A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000553535.2:n.248+2449A>T | ||
| ENST00000554986.2:c.42-2909A>T | ENSP00000452700.2:n.42-2909A>T | |
| ENST00000555955.3:n.1197+2449A>T | ||
| XM_017021602.2:c.-297A>T | XP_016877091.1:n.-297A>T |