Linked Data
dbSNP Id:
rs1567746480
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.66240099G>A , CM000679.2:g.66240099G>A | GRCh38 |
| NC_000017.10:g.64236217G>A , CM000679.1:g.64236217G>A | GRCh37 |
| NC_000017.9:g.61666679G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000577982.1:c.-43-10677C>T | ENSP00000464301.1:n.-43-10677C>T |